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	<title>NGS &#8211; GenoMed</title>
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	<title>NGS &#8211; GenoMed</title>
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	<item>
		<title>Arritmias cardíacas: painel de genes por NGS</title>
		<link>https://genomed.pt/arritmias-cardiacas-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 02:18:41 +0000</pubDate>
				<category><![CDATA[Cardiologia]]></category>
		<category><![CDATA[Cardiologia Pediátrica]]></category>
		<category><![CDATA[Medicina Interna]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Reumatologia]]></category>
		<category><![CDATA[PTDGF2]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20316</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Arritmias cardíacas: painel de genes por NGS" data-especialidade-1="Cardiologia" data-especialidade-2="Cardiologia Pediátrica, Medicina Interna, Reumatologia" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="202" data-lista-genes="A2ML1, AARS2, ABCC9, ACAD9, ACADVL, ACTA1, ACTC1, ACTN2, AGK, AGL, AGPAT2, AKAP9, ALMS1, ANK2, ANKRD1, ANO5, ATP5E, ATPAF2, BAG3, BRAF, BSCL2, CACNA1C, CACNA1D, CACNA2D1, CALM1, CALM2, CALM3, CALR3, CAPN3, CASQ2, CAV3, CAVIN4, CDH2 ,CHRM2, COA5, COA6, COQ2, COX15, COX6B1, CRYAB, CSRP3, CTNNA3, DES, DLD, DMD, DNAJC19, DOLK, DPP6, DSC2, DSG2, DSG3, DSP, DTNA, ELAC2, EMD, EYA4, FAH, FHL1, FHL2, FHOD3, FKRP, FKTN, FLNC, FOXRED1, FXN, GAA, GATA4, GATA6, GATAD1, GFM1, GJA1, GJA5, GLA, GLB1, GNPTAB, GPD1L, GUSB, HCN4, HRAS, JPH2, JUP, KCNA1, KCNA5, KCND2, KCND3, KCNE1, KCNE2, KCNE3, KCNE5, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNK17, KCNK3, KCNQ1, KCNQ2, KCNT1, KRAS, LAMA2, LAMA4, LAMP2, LDB3, LDLR, LIAS, LMNA, LZTR1, MAP2K1, MAP2K2, MIB1, MLYCD, MRPL3, MRPL44, MRPS22, MTO1, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYL4, MYOM1, MYOT, MYOZ2, MYPN, NEBL, NEXN, NF1, NKX2-5, NKX2-6, NNT, NPPA, NRAS, OBSCN, PDHA1, PDLIM3, PHKA1, PITX2, PKP2, PLN, PMM2, PPA2, PRDM16, PRKAG2, PSEN1, PSEN2, PTPN11, RAF1, RANGRF, RASA2, RBM20, RIT1, RRAS, RYR2, SCN1A, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SCN9A, SCO2, SDHA, SEMA3A, SGCD, SHOC2, SLC22A5, SLC25A3, SLC25A4, SLMAP, SNTA1, SOS1, SOS2, SPEG, SPRED1, SURF1, SYNE1, SYNE2, TAZ, TBX20, TBX5, TCAP, TGFB3, TJP1, TMEM43, TMEM70, TMPO, TNNC1, TNNI3, TNNI3K, TNNT2, TOR1AIP1, TPM1, TRDN, TRIM63, TRPM4, TSFM, TTN, TTR, TXNRD2, VCL, XK" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Cardiologia</p>
<p> Cardiologia Pediátrica, Medicina Interna, Reumatologia</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204290358" >				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Metodologia</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204252853" >
		<div class="wpb_wrapper">
			<p>						NGS, com CNVs					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Código SNS</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204015375" >
		<div class="wpb_wrapper">
			<p>						34900					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						&#8211;					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						202					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						A2ML1, AARS2, ABCC9, ACAD9, ACADVL, ACTA1, ACTC1, ACTN2, AGK, AGL, AGPAT2, AKAP9, ALMS1, ANK2, ANKRD1, ANO5, ATP5E, ATPAF2, BAG3, BRAF, BSCL2, CACNA1C, CACNA1D, CACNA2D1, CALM1, CALM2, CALM3, CALR3, CAPN3, CASQ2, CAV3, CAVIN4, CDH2 ,CHRM2, COA5, COA6, COQ2, COX15, COX6B1, CRYAB, CSRP3, CTNNA3, DES, DLD, DMD, DNAJC19, DOLK, DPP6, DSC2, DSG2, DSG3, DSP, DTNA, ELAC2, EMD, EYA4, FAH, FHL1, FHL2, FHOD3, FKRP, FKTN, FLNC, FOXRED1, FXN, GAA, GATA4, GATA6, GATAD1, GFM1, GJA1, GJA5, GLA, GLB1, GNPTAB, GPD1L, GUSB, HCN4, HRAS, JPH2, JUP, KCNA1, KCNA5, KCND2, KCND3, KCNE1, KCNE2, KCNE3, KCNE5, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNK17, KCNK3, KCNQ1, KCNQ2, KCNT1, KRAS, LAMA2, LAMA4, LAMP2, LDB3, LDLR, LIAS, LMNA, LZTR1, MAP2K1, MAP2K2, MIB1, MLYCD, MRPL3, MRPL44, MRPS22, MTO1, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYL4, MYOM1, MYOT, MYOZ2, MYPN, NEBL, NEXN, NF1, NKX2-5, NKX2-6, NNT, NPPA, NRAS, OBSCN, PDHA1, PDLIM3, PHKA1, PITX2, PKP2, PLN, PMM2, PPA2, PRDM16, PRKAG2, PSEN1, PSEN2, PTPN11, RAF1, RANGRF, RASA2, RBM20, RIT1, RRAS, RYR2, SCN1A, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SCN9A, SCO2, SDHA, SEMA3A, SGCD, SHOC2, SLC22A5, SLC25A3, SLC25A4, SLMAP, SNTA1, SOS1, SOS2, SPEG, SPRED1, SURF1, SYNE1, SYNE2, TAZ, TBX20, TBX5, TCAP, TGFB3, TJP1, TMEM43, TMEM70, TMPO, TNNC1, TNNI3, TNNI3K, TNNT2, TOR1AIP1, TPM1, TRDN, TRIM63, TRPM4, TSFM, TTN, TTR, TXNRD2, VCL, XK					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >TAT</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267243061" >
		<div class="wpb_wrapper">
			<p>						2 a 3 meses					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>					<h6 style="text-align: left" class="vc_custom_heading" >Tipo de Amostra</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267463385" >
		<div class="wpb_wrapper">
			<p>						Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado<br />
 ou<br />
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>				</div></div></div>			</div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591277235133 mkdf-content-aligment-left" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<a itemprop="url" href="https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf" target="_blank"  class="mkdf-btn mkdf-btn-medium mkdf-btn-solid mkdf-btn-solid-dark mkdf-btn-icon"  >
    <span class="mkdf-btn-text">Requisitar</span>
    <span class="mkdf-btn-icon-holder">
        <span class="mkdf-btn-icon-normal" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
        <span class="mkdf-btn-icon-flip" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
    </span>
</a>				</div></div></div>			</div>		</div></div></div>	</div>
]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Cútis laxa: painel de genes por NGS</title>
		<link>https://genomed.pt/cutis-laxa-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 02:26:41 +0000</pubDate>
				<category><![CDATA[Cardiologia]]></category>
		<category><![CDATA[Dermatologia]]></category>
		<category><![CDATA[Medicina Interna]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[Reumatologia]]></category>
		<category><![CDATA[PTDGF55]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20528</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Cútis laxa: painel de genes por NGS" data-especialidade-1="Dermatologia" data-especialidade-2="Cardiologia, Medicina Interna, Pediatria, Reumatologia" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="15" data-lista-genes="ALDH18A1, ATP6V0A2, ATP7A, C1R, COL11A1, EFEMP2, ELN, FBLN5, FLNA, GORAB, LTBP4, PLAC8, PTDSS1, PYCR1, RIN2" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Dermatologia</p>
<p> Cardiologia, Medicina Interna, Pediatria, Reumatologia</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204290358" >				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Metodologia</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204252853" >
		<div class="wpb_wrapper">
			<p>						NGS, com CNVs					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Código SNS</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204015375" >
		<div class="wpb_wrapper">
			<p>						34900					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						&#8211;					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						15					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						ALDH18A1, ATP6V0A2, ATP7A, C1R, COL11A1, EFEMP2, ELN, FBLN5, FLNA, GORAB, LTBP4, PLAC8, PTDSS1, PYCR1, RIN2					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >TAT</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267243061" >
		<div class="wpb_wrapper">
			<p>						2 a 3 meses					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>					<h6 style="text-align: left" class="vc_custom_heading" >Tipo de Amostra</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267463385" >
		<div class="wpb_wrapper">
			<p>						Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado<br />
 ou<br />
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>				</div></div></div>			</div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591277235133 mkdf-content-aligment-left" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<a itemprop="url" href="https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf" target="_blank"  class="mkdf-btn mkdf-btn-medium mkdf-btn-solid mkdf-btn-solid-dark mkdf-btn-icon"  >
    <span class="mkdf-btn-text">Requisitar</span>
    <span class="mkdf-btn-icon-holder">
        <span class="mkdf-btn-icon-normal" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
        <span class="mkdf-btn-icon-flip" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
    </span>
</a>				</div></div></div>			</div>		</div></div></div>	</div>
]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Doença inflamatória intestinal: painel de genes por NGS</title>
		<link>https://genomed.pt/doenca-inflamatoria-intestinal-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 02:29:58 +0000</pubDate>
				<category><![CDATA[Doenças do Sistema Imunitário]]></category>
		<category><![CDATA[Gastroenterologia]]></category>
		<category><![CDATA[Imunodeficiências]]></category>
		<category><![CDATA[Medicina Interna]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[Reumatologia]]></category>
		<category><![CDATA[PTDGF86]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20532</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Doença inflamatória intestinal: painel de genes por NGS" data-especialidade-1="Doenças do Sistema Imunitário" data-especialidade-2="Pediatria, Imunodeficiências, Reumatologia, Gastroenterologia, Medicina Interna" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="55" data-lista-genes="ADA, ADAM17, AICDA, BTK, CD3G, CD40LG, CTLA4, CYBA, CYBB, DCLRE1C, DKC1, DOCK8, EPCAM, FOXP3, G6PC3, ICOS, IL10, IL10RA, IL10RB, IL21, IL2RA, IL2RG, ITGB2, LIG4, LRBA, MALT1, MEFV, MVK, MYO5B, NCF1, NCF2, NCF4, NEUROG3, NFAT5, NLRC4, NOD2, PIK3CD, PIK3R1, PLCG2, RAG1, RAG2, RTEL1, SH2D1A, SI, SKIV2L, SLC37A4, STAT1, STAT3, STIM1, STXBP2, TTC37, TTC7A, WAS, XIAP, ZAP70" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Doenças do Sistema Imunitário</p>
<p> Pediatria, Imunodeficiências, Reumatologia, Gastroenterologia, Medicina Interna</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204290358" >				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Metodologia</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204252853" >
		<div class="wpb_wrapper">
			<p>						NGS, com CNVs					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Código SNS</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204015375" >
		<div class="wpb_wrapper">
			<p>						34900					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						&#8211;					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						55					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						ADA, ADAM17, AICDA, BTK, CD3G, CD40LG, CTLA4, CYBA, CYBB, DCLRE1C, DKC1, DOCK8, EPCAM, FOXP3, G6PC3, ICOS, IL10, IL10RA, IL10RB, IL21, IL2RA, IL2RG, ITGB2, LIG4, LRBA, MALT1, MEFV, MVK, MYO5B, NCF1, NCF2, NCF4, NEUROG3, NFAT5, NLRC4, NOD2, PIK3CD, PIK3R1, PLCG2, RAG1, RAG2, RTEL1, SH2D1A, SI, SKIV2L, SLC37A4, STAT1, STAT3, STIM1, STXBP2, TTC37, TTC7A, WAS, XIAP, ZAP70					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >TAT</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267243061" >
		<div class="wpb_wrapper">
			<p>						2 a 3 meses					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>					<h6 style="text-align: left" class="vc_custom_heading" >Tipo de Amostra</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267463385" >
		<div class="wpb_wrapper">
			<p>						Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado<br />
 ou<br />
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>				</div></div></div>			</div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591277235133 mkdf-content-aligment-left" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<a itemprop="url" href="https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf" target="_blank"  class="mkdf-btn mkdf-btn-medium mkdf-btn-solid mkdf-btn-solid-dark mkdf-btn-icon"  >
    <span class="mkdf-btn-text">Requisitar</span>
    <span class="mkdf-btn-icon-holder">
        <span class="mkdf-btn-icon-normal" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
        <span class="mkdf-btn-icon-flip" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
    </span>
</a>				</div></div></div>			</div>		</div></div></div>	</div>
]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Doenças auto-inflamatórias: painel de genes por NGS</title>
		<link>https://genomed.pt/doencas-auto-inflamatorias-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 03:43:07 +0000</pubDate>
				<category><![CDATA[Doenças do Sistema Imunitário]]></category>
		<category><![CDATA[Medicina Interna]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[Reumatologia]]></category>
		<category><![CDATA[PTDGF88]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20796</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Doenças auto-inflamatórias: painel de genes por NGS" data-especialidade-1="Doenças do Sistema Imunitário" data-especialidade-2="Reumatologia, Pediatria, Medicina Interna" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="105" data-lista-genes="ADA, ADA2, ADAM17, ADAR, AICDA, AP1S3, AP3B1, ASAH1, BLOC1S6, BTK, CARD14, CASP10, CASP8, CD27, CD3G, CD40LG, CTLA4, CYBA, CYBB, DCLRE1C, DDX58, DKC1, DOCK8, ELANE, EPCAM, FADD, FARSA, FAS, FASLG, FOXP3, G6PC3, HAX1, ICOS, IFIH1, IL10, IL10RA, IL10RB, IL1RN, IL21, IL2RA, IL2RG, IL36RN, ITGB2, ITK, KRAS, LIG4, LPIN2, LRBA, LYST, MAGT1, MALT1, MEFV, MVK, MYO5B, NCF1, NCF2, NCF4, NEUROG3, NFAT5, NLRC4, NLRP1, NLRP12, NLRP3, NOD2, NRAS, OTULIN, PIK3CD, PIK3R1, PLCG2, PRF1, PRKCD, PSMB8, PSTPIP1, RAB27A, RAG1, RAG2, RASGRP1, RBCK1, RNASEH2A, RNASEH2B, RNASEH2C, RTEL1, SAMHD1, SH2D1A, SI, SKIV2L, SLC29A3, SLC37A4, SLC7A7, STAT1, STAT3, STIM1, STX11, STXBP2, TMEM173, TNFAIP3, TNFRSF11A, TNFRSF1A, TREX1, TTC37, TTC7A, UNC13D, WAS, XIAP, ZAP70" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Doenças do Sistema Imunitário</p>
<p> Reumatologia, Pediatria, Medicina Interna</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204290358" >				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Metodologia</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204252853" >
		<div class="wpb_wrapper">
			<p>						NGS, com CNVs					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Código SNS</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204015375" >
		<div class="wpb_wrapper">
			<p>						34900					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						&#8211;					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						105					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						ADA, ADA2, ADAM17, ADAR, AICDA, AP1S3, AP3B1, ASAH1, BLOC1S6, BTK, CARD14, CASP10, CASP8, CD27, CD3G, CD40LG, CTLA4, CYBA, CYBB, DCLRE1C, DDX58, DKC1, DOCK8, ELANE, EPCAM, FADD, FARSA, FAS, FASLG, FOXP3, G6PC3, HAX1, ICOS, IFIH1, IL10, IL10RA, IL10RB, IL1RN, IL21, IL2RA, IL2RG, IL36RN, ITGB2, ITK, KRAS, LIG4, LPIN2, LRBA, LYST, MAGT1, MALT1, MEFV, MVK, MYO5B, NCF1, NCF2, NCF4, NEUROG3, NFAT5, NLRC4, NLRP1, NLRP12, NLRP3, NOD2, NRAS, OTULIN, PIK3CD, PIK3R1, PLCG2, PRF1, PRKCD, PSMB8, PSTPIP1, RAB27A, RAG1, RAG2, RASGRP1, RBCK1, RNASEH2A, RNASEH2B, RNASEH2C, RTEL1, SAMHD1, SH2D1A, SI, SKIV2L, SLC29A3, SLC37A4, SLC7A7, STAT1, STAT3, STIM1, STX11, STXBP2, TMEM173, TNFAIP3, TNFRSF11A, TNFRSF1A, TREX1, TTC37, TTC7A, UNC13D, WAS, XIAP, ZAP70					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >TAT</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267243061" >
		<div class="wpb_wrapper">
			<p>						2 a 3 meses					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>					<h6 style="text-align: left" class="vc_custom_heading" >Tipo de Amostra</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267463385" >
		<div class="wpb_wrapper">
			<p>						Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado<br />
 ou<br />
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>				</div></div></div>			</div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591277235133 mkdf-content-aligment-left" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<a itemprop="url" href="https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf" target="_blank"  class="mkdf-btn mkdf-btn-medium mkdf-btn-solid mkdf-btn-solid-dark mkdf-btn-icon"  >
    <span class="mkdf-btn-text">Requisitar</span>
    <span class="mkdf-btn-icon-holder">
        <span class="mkdf-btn-icon-normal" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
        <span class="mkdf-btn-icon-flip" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
    </span>
</a>				</div></div></div>			</div>		</div></div></div>	</div>
]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Doenças da aorta / tecido conjuntivo: painel de genes por NGS (painel alargado)</title>
		<link>https://genomed.pt/doencas-da-aorta-tecido-conjuntivo-painel-de-genes-por-ngs-painel-alargado/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Tue, 08 Sep 2020 01:12:09 +0000</pubDate>
				<category><![CDATA[Angiologia e Cirurgia Vascular]]></category>
		<category><![CDATA[Cardiologia]]></category>
		<category><![CDATA[Cardiologia Pediátrica]]></category>
		<category><![CDATA[Cirurgia Cardiotorácica]]></category>
		<category><![CDATA[Medicina Interna]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Reumatologia]]></category>
		<category><![CDATA[PTDGF542]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=31168</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Doenças da aorta / tecido conjuntivo: painel de genes por NGS (painel alargado)" data-especialidade-1="Cardiologia" data-especialidade-2="Cardiologia Pediátrica, Angiologia e Cirurgia Vascular, Cirurgia Cardiotorácica, Medicina Interna, Reumatologia" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="122" data-lista-genes="ABCC6, ABL1, ACTA2, ACVR1, ADAMTS10, ADAMTS17, ADAMTS2, ADAMTSL4, AEBP1, ALDH18A1, ALPL, ARHGAP31, ATP6V0A2, ATP6V1A, ATP6V1E1, ATP7A, B3GALT6, B3GAT3, B3GLCT, B4GALT7, BGN, BMP1, BMP4, C1R, C1S, CBS, CHST14, COL11A1, COL11A2, COL12A1, COL18A1, COL1A1, COL1A2, COL2A1, COL3A1, COL4A1, COL5A1, COL5A2, COL6A1, COL6A2, COL6A3, COL9A1, COL9A2, COL9A3, COX7B, CREB3L1, CRTAP, DCC, DLL4, DOCK6, DSE, EFEMP2, ELN, EMILIN1, EOGT, FBLN5, FBN1, FBN2, FKBP10, FKBP14, FLCN, FLNA, FOXE3, GAA, GGCX, GZF1, IPO8, GORAB, GYPC, HRAS, IFITM5, KCNJ8, KIF22, LOX, LRP5, LTBP2, LTBP4, MAT2A, MED12, MFAP5, MYH11, MYLK, NOTCH1, P3H1, PIEZO2, PLOD1, PLOD2, PLOD3, PLS3, PPIB, PRDM5, PRKG1, PTPN11, PYCR1, RBPJ, RET, RIN2, ROBO3, SERPINF1, SERPINH1, SGMS2, SKI, SLC2A10, SLC39A13, SMAD2, SMAD3, SMAD4, SMAD6, SP7, SPARC, TAB2, TGFB2, TGFB3, TGFBR1, TGFBR2, THBS2, TMEM38B, TNXB, VCAN, WNT1, ZNF469" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Cardiologia</p>
<p> Cardiologia Pediátrica, Angiologia e Cirurgia Vascular, Cirurgia Cardiotorácica, Medicina Interna, Reumatologia</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204290358" >				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Metodologia</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204252853" >
		<div class="wpb_wrapper">
			<p>						NGS, com CNVs					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Código SNS</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204015375" >
		<div class="wpb_wrapper">
			<p>						34900					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						&#8211;					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						122					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						ABCC6, ABL1, ACTA2, ACVR1, ADAMTS10, ADAMTS17, ADAMTS2, ADAMTSL4, AEBP1, ALDH18A1, ALPL, ARHGAP31, ATP6V0A2, ATP6V1A, ATP6V1E1, ATP7A, B3GALT6, B3GAT3, B3GLCT, B4GALT7, BGN, BMP1, BMP4, C1R, C1S, CBS, CHST14, COL11A1, COL11A2, COL12A1, COL18A1, COL1A1, COL1A2, COL2A1, COL3A1, COL4A1, COL5A1, COL5A2, COL6A1, COL6A2, COL6A3, COL9A1, COL9A2, COL9A3, COX7B, CREB3L1, CRTAP, DCC, DLL4, DOCK6, DSE, EFEMP2, ELN, EMILIN1, EOGT, FBLN5, FBN1, FBN2, FKBP10, FKBP14, FLCN, FLNA, FOXE3, GAA, GGCX, GZF1, IPO8, GORAB, GYPC, HRAS, IFITM5, KCNJ8, KIF22, LOX, LRP5, LTBP2, LTBP4, MAT2A, MED12, MFAP5, MYH11, MYLK, NOTCH1, P3H1, PIEZO2, PLOD1, PLOD2, PLOD3, PLS3, PPIB, PRDM5, PRKG1, PTPN11, PYCR1, RBPJ, RET, RIN2, ROBO3, SERPINF1, SERPINH1, SGMS2, SKI, SLC2A10, SLC39A13, SMAD2, SMAD3, SMAD4, SMAD6, SP7, SPARC, TAB2, TGFB2, TGFB3, TGFBR1, TGFBR2, THBS2, TMEM38B, TNXB, VCAN, WNT1, ZNF469					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >TAT</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267243061" >
		<div class="wpb_wrapper">
			<p>						2 a 3 meses					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>					<h6 style="text-align: left" class="vc_custom_heading" >Tipo de Amostra</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267463385" >
		<div class="wpb_wrapper">
			<p>						Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado<br />
 ou<br />
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>				</div></div></div>			</div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591277235133 mkdf-content-aligment-left" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<a itemprop="url" href="https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf" target="_blank"  class="mkdf-btn mkdf-btn-medium mkdf-btn-solid mkdf-btn-solid-dark mkdf-btn-icon"  >
    <span class="mkdf-btn-text">Requisitar</span>
    <span class="mkdf-btn-icon-holder">
        <span class="mkdf-btn-icon-normal" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
        <span class="mkdf-btn-icon-flip" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
    </span>
</a>				</div></div></div>			</div>		</div></div></div>	</div>
]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Doenças da aorta / tecido conjuntivo: painel de genes por NGS (painel básico)</title>
		<link>https://genomed.pt/doencas-da-aorta-tecido-conjuntivo-painel-de-genes-por-ngs-2/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Sat, 15 Aug 2020 00:02:04 +0000</pubDate>
				<category><![CDATA[Angiologia e Cirurgia Vascular]]></category>
		<category><![CDATA[Cardiologia]]></category>
		<category><![CDATA[Cardiologia Pediátrica]]></category>
		<category><![CDATA[Cirurgia Cardiotorácica]]></category>
		<category><![CDATA[Medicina Interna]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Reumatologia]]></category>
		<category><![CDATA[PTDGF5]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=22505</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Doenças da aorta / tecido conjuntivo: painel de genes por NGS (painel básico)" data-especialidade-1="Cardiologia" data-especialidade-2="Cardiologia Pediátrica, Angiologia e Cirurgia Vascular, Cirurgia Cardiotorácica, Medicina Interna, Reumatologia" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="65" data-lista-genes="ABL1, ACTA2, ADAMTS10, ADAMTS17, ADAMTS2, ADAMTSL4, ATP7A, B3GALT6, B3GLCT, B4GALT7, BGN, C1R, C1S, CBS, CHST14, COL11A1, COL11A2, COL12A1, COL1A1, COL1A2, COL2A1, COL3A1, COL4A1, COL5A1, COL5A2, COL9A1, COL9A2, DSE, EFEMP2, ELN, FBN1, FBN2, FKBP14, FLCN, FLNA, FOXE3, GAA, HRAS, IPO8, KCNJ8, LOX, LTBP2, MAT2A, MED12, MFAP5, MYH11, MYLK, NOTCH1, PLOD1, PRDM5, PRKG1, PTPN11, SKI, SLC2A10, SLC39A13, SMAD2, SMAD3, SMAD4, TGFB2, TGFB3, TGFBR1, TGFBR2, THBS2, TNXB, ZNF469" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Cardiologia</p>
<p> Cardiologia Pediátrica, Angiologia e Cirurgia Vascular, Cirurgia Cardiotorácica, Medicina Interna, Reumatologia</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204290358" >				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Metodologia</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204252853" >
		<div class="wpb_wrapper">
			<p>						NGS, com CNVs					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Código SNS</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204015375" >
		<div class="wpb_wrapper">
			<p>						34900					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						&#8211;					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						65					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						ABL1, ACTA2, ADAMTS10, ADAMTS17, ADAMTS2, ADAMTSL4, ATP7A, B3GALT6, B3GLCT, B4GALT7, BGN, C1R, C1S, CBS, CHST14, COL11A1, COL11A2, COL12A1, COL1A1, COL1A2, COL2A1, COL3A1, COL4A1, COL5A1, COL5A2, COL9A1, COL9A2, DSE, EFEMP2, ELN, FBN1, FBN2, FKBP14, FLCN, FLNA, FOXE3, GAA, HRAS, IPO8, KCNJ8, LOX, LTBP2, MAT2A, MED12, MFAP5, MYH11, MYLK, NOTCH1, PLOD1, PRDM5, PRKG1, PTPN11, SKI, SLC2A10, SLC39A13, SMAD2, SMAD3, SMAD4, TGFB2, TGFB3, TGFBR1, TGFBR2, THBS2, TNXB, ZNF469					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >TAT</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267243061" >
		<div class="wpb_wrapper">
			<p>						2 a 3 meses					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>					<h6 style="text-align: left" class="vc_custom_heading" >Tipo de Amostra</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267463385" >
		<div class="wpb_wrapper">
			<p>						Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado<br />
 ou<br />
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>				</div></div></div>			</div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591277235133 mkdf-content-aligment-left" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<a itemprop="url" href="https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf" target="_blank"  class="mkdf-btn mkdf-btn-medium mkdf-btn-solid mkdf-btn-solid-dark mkdf-btn-icon"  >
    <span class="mkdf-btn-text">Requisitar</span>
    <span class="mkdf-btn-icon-holder">
        <span class="mkdf-btn-icon-normal" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
        <span class="mkdf-btn-icon-flip" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
    </span>
</a>				</div></div></div>			</div>		</div></div></div>	</div>
]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Febres recorrentes: painel de genes por NGS</title>
		<link>https://genomed.pt/febres-recorrentes-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 02:30:32 +0000</pubDate>
				<category><![CDATA[Doenças do Sistema Imunitário]]></category>
		<category><![CDATA[Imunodeficiências]]></category>
		<category><![CDATA[Medicina Interna]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[Reumatologia]]></category>
		<category><![CDATA[PTDGF91]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20536</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Febres recorrentes: painel de genes por NGS" data-especialidade-1="Doenças do Sistema Imunitário" data-especialidade-2="Pediatria, Imunodeficiências, Reumatologia, Medicina Interna" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="35" data-lista-genes="ADAR, AP1S3, ASAH1, CARD14, DDX58, ELANE, HAX1, IFIH1, IL10RA, IL10RB, IL1RN, IL36RN, LPIN2, MEFV, MVK, NLRC4, NLRP1, NLRP12, NLRP3, NOD2, OTULIN, PLCG2, PSMB8, PSTPIP1, RBCK1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, SLC29A3, TMEM173, TNFAIP3, TNFRSF11A, TNFRSF1A, TREX1" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Doenças do Sistema Imunitário</p>
<p> Pediatria, Imunodeficiências, Reumatologia, Medicina Interna</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204290358" >				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Metodologia</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204252853" >
		<div class="wpb_wrapper">
			<p>						NGS, com CNVs					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Código SNS</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204015375" >
		<div class="wpb_wrapper">
			<p>						34900					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						&#8211;					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						35					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						ADAR, AP1S3, ASAH1, CARD14, DDX58, ELANE, HAX1, IFIH1, IL10RA, IL10RB, IL1RN, IL36RN, LPIN2, MEFV, MVK, NLRC4, NLRP1, NLRP12, NLRP3, NOD2, OTULIN, PLCG2, PSMB8, PSTPIP1, RBCK1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, SLC29A3, TMEM173, TNFAIP3, TNFRSF11A, TNFRSF1A, TREX1					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >TAT</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267243061" >
		<div class="wpb_wrapper">
			<p>						2 a 3 meses					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>					<h6 style="text-align: left" class="vc_custom_heading" >Tipo de Amostra</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267463385" >
		<div class="wpb_wrapper">
			<p>						Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado<br />
 ou<br />
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>				</div></div></div>			</div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591277235133 mkdf-content-aligment-left" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<a itemprop="url" href="https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf" target="_blank"  class="mkdf-btn mkdf-btn-medium mkdf-btn-solid mkdf-btn-solid-dark mkdf-btn-icon"  >
    <span class="mkdf-btn-text">Requisitar</span>
    <span class="mkdf-btn-icon-holder">
        <span class="mkdf-btn-icon-normal" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
        <span class="mkdf-btn-icon-flip" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
    </span>
</a>				</div></div></div>			</div>		</div></div></div>	</div>
]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Miocardiopatia hipertrófica: painel de genes por NGS (genes sarcoméricos)</title>
		<link>https://genomed.pt/miocardiopatia-hipertrofica-painel-de-genes-por-ngs-genes-sarcomericos/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 02:23:12 +0000</pubDate>
				<category><![CDATA[Cardiologia]]></category>
		<category><![CDATA[Cardiologia Pediátrica]]></category>
		<category><![CDATA[Medicina Interna]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Reumatologia]]></category>
		<category><![CDATA[PTDGF32]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20436</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Miocardiopatia hipertrófica: painel de genes por NGS (genes sarcoméricos)" data-especialidade-1="Cardiologia" data-especialidade-2="Cardiologia Pediátrica, Medicina Interna, Reumatologia" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="PS192600" data-num-genes="8" data-lista-genes="ACTC1, MYBPC3, MYH7, MYL2, MYL3, TNNI3, TNNT2, TPM1" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Cardiologia</p>
<p> Cardiologia Pediátrica, Medicina Interna, Reumatologia</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204290358" >				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Metodologia</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204252853" >
		<div class="wpb_wrapper">
			<p>						NGS, com CNVs					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Código SNS</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204015375" >
		<div class="wpb_wrapper">
			<p>						34900					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						<a href='https://www.omim.org/phenotypicSeries/PS192600' target='_blank' rel="noopener">PS192600</a>					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						8					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						ACTC1, MYBPC3, MYH7, MYL2, MYL3, TNNI3, TNNT2, TPM1					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >TAT</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267243061" >
		<div class="wpb_wrapper">
			<p>						2 a 3 meses					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>					<h6 style="text-align: left" class="vc_custom_heading" >Tipo de Amostra</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267463385" >
		<div class="wpb_wrapper">
			<p>						Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado<br />
 ou<br />
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>				</div></div></div>			</div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591277235133 mkdf-content-aligment-left" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<a itemprop="url" href="https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf" target="_blank"  class="mkdf-btn mkdf-btn-medium mkdf-btn-solid mkdf-btn-solid-dark mkdf-btn-icon"  >
    <span class="mkdf-btn-text">Requisitar</span>
    <span class="mkdf-btn-icon-holder">
        <span class="mkdf-btn-icon-normal" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
        <span class="mkdf-btn-icon-flip" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
    </span>
</a>				</div></div></div>			</div>		</div></div></div>	</div>
]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Miocardiopatia hipertrófica: painel de genes por NGS (painel alargado)</title>
		<link>https://genomed.pt/miocardiopatia-hipertrofica-painel-de-genes-por-ngs-painel-alargado/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 02:23:21 +0000</pubDate>
				<category><![CDATA[Cardiologia]]></category>
		<category><![CDATA[Cardiologia Pediátrica]]></category>
		<category><![CDATA[Medicina Interna]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Reumatologia]]></category>
		<category><![CDATA[PTDGF33]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20440</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Miocardiopatia hipertrófica: painel de genes por NGS (painel alargado)" data-especialidade-1="Cardiologia" data-especialidade-2="Cardiologia Pediátrica, Medicina Interna, Reumatologia" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="PS192600" data-num-genes="86" data-lista-genes="A2ML1, AARS2, ACADVL, ACTA1, ACTC1, ACTN2, AGL, ALPK3, ANKRD1, ATP5E, BAG3, BRAF, CACNA1C, CALR3, CASQ2, CAV3, CBL, COA5, CPT2, CRYAB, CSRP3, DES, ELAC2, FHL1, FHOD3, FLNC, FOXRED1, FXN, GAA, GATA4, GLA, GLB1, GUSB, HRAS, JPH2, KCNQ1, KLF10, KRAS, LAMP2, LDB3, LMNA, MAP2K1, MAP2K2, MRPL3, MTO1, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYO6, MYOM1, MYOZ2, MYPN, NEXN, NF1, NRAS, OBSCN, PDLIM3, PLN, PRKAG2, PTPN11, RAF1, RASA1, RIT1, RRAS, RYR2, SCO2, SHOC2, SLC25A3, SLC25A4, SOS1, SOS2, SPRED1, TCAP, TMEM70, TNNC1, TNNI3, TNNT2, TPM1, TRIM63, TSFM, TTN, TTR, VCL" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Cardiologia</p>
<p> Cardiologia Pediátrica, Medicina Interna, Reumatologia</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204290358" >				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Metodologia</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204252853" >
		<div class="wpb_wrapper">
			<p>						NGS, com CNVs					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Código SNS</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204015375" >
		<div class="wpb_wrapper">
			<p>						34900					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						<a href='https://www.omim.org/phenotypicSeries/PS192600' target='_blank' rel="noopener">PS192600</a>					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						86					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						A2ML1, AARS2, ACADVL, ACTA1, ACTC1, ACTN2, AGL, ALPK3, ANKRD1, ATP5E, BAG3, BRAF, CACNA1C, CALR3, CASQ2, CAV3, CBL, COA5, CPT2, CRYAB, CSRP3, DES, ELAC2, FHL1, FHOD3, FLNC, FOXRED1, FXN, GAA, GATA4, GLA, GLB1, GUSB, HRAS, JPH2, KCNQ1, KLF10, KRAS, LAMP2, LDB3, LMNA, MAP2K1, MAP2K2, MRPL3, MTO1, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYO6, MYOM1, MYOZ2, MYPN, NEXN, NF1, NRAS, OBSCN, PDLIM3, PLN, PRKAG2, PTPN11, RAF1, RASA1, RIT1, RRAS, RYR2, SCO2, SHOC2, SLC25A3, SLC25A4, SOS1, SOS2, SPRED1, TCAP, TMEM70, TNNC1, TNNI3, TNNT2, TPM1, TRIM63, TSFM, TTN, TTR, VCL					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >TAT</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267243061" >
		<div class="wpb_wrapper">
			<p>						2 a 3 meses					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>					<h6 style="text-align: left" class="vc_custom_heading" >Tipo de Amostra</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267463385" >
		<div class="wpb_wrapper">
			<p>						Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado<br />
 ou<br />
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>				</div></div></div>			</div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591277235133 mkdf-content-aligment-left" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<a itemprop="url" href="https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf" target="_blank"  class="mkdf-btn mkdf-btn-medium mkdf-btn-solid mkdf-btn-solid-dark mkdf-btn-icon"  >
    <span class="mkdf-btn-text">Requisitar</span>
    <span class="mkdf-btn-icon-holder">
        <span class="mkdf-btn-icon-normal" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
        <span class="mkdf-btn-icon-flip" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
    </span>
</a>				</div></div></div>			</div>		</div></div></div>	</div>
]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Miocardiopatia hipertrófica: painel de genes por NGS (painel básico)</title>
		<link>https://genomed.pt/miocardiopatia-hipertrofica-painel-de-genes-por-ngs-painel-basico/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 02:23:30 +0000</pubDate>
				<category><![CDATA[Cardiologia]]></category>
		<category><![CDATA[Cardiologia Pediátrica]]></category>
		<category><![CDATA[Medicina Interna]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Reumatologia]]></category>
		<category><![CDATA[PTDGF34]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20444</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Miocardiopatia hipertrófica: painel de genes por NGS (painel básico)" data-especialidade-1="Cardiologia" data-especialidade-2="Cardiologia Pediátrica, Medicina Interna, Reumatologia" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="PS192600" data-num-genes="25" data-lista-genes="ACTC1, ACTN2, ALPK3, CACNA1C, CSRP3, FHL1, FHOD3, FLNC, GLA, LAMP2, MYBPC3, MYH7, MYL2, MYL3, PLN, PRKAG2, PTPN11, RAF1, RIT1, TNNC1, TNNI3, TNNT2, TPM1, TRIM63, TTR" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Cardiologia</p>
<p> Cardiologia Pediátrica, Medicina Interna, Reumatologia</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204290358" >				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Metodologia</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204252853" >
		<div class="wpb_wrapper">
			<p>						NGS, com CNVs					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Código SNS</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204015375" >
		<div class="wpb_wrapper">
			<p>						34900					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						<a href='https://www.omim.org/phenotypicSeries/PS192600' target='_blank' rel="noopener">PS192600</a>					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						25					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						ACTC1, ACTN2, ALPK3, CACNA1C, CSRP3, FHL1, FHOD3, FLNC, GLA, LAMP2, MYBPC3, MYH7, MYL2, MYL3, PLN, PRKAG2, PTPN11, RAF1, RIT1, TNNC1, TNNI3, TNNT2, TPM1, TRIM63, TTR					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >TAT</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267243061" >
		<div class="wpb_wrapper">
			<p>						2 a 3 meses					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>					<h6 style="text-align: left" class="vc_custom_heading" >Tipo de Amostra</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591267463385" >
		<div class="wpb_wrapper">
			<p>						Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado<br />
 ou<br />
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.					</p>

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>				</div></div></div>			</div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591277235133 mkdf-content-aligment-left" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<a itemprop="url" href="https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf" target="_blank"  class="mkdf-btn mkdf-btn-medium mkdf-btn-solid mkdf-btn-solid-dark mkdf-btn-icon"  >
    <span class="mkdf-btn-text">Requisitar</span>
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        <span class="mkdf-btn-icon-normal" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
        <span class="mkdf-btn-icon-flip" ><i class="mkdf-icon-font-awesome fa fa-download " ></i></span>
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