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	<title>NGS &#8211; GenoMed</title>
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	<title>NGS &#8211; GenoMed</title>
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	<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>
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]]></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>Síndrome auto-Inflamatória familiar, Behcet-like: gene TNFAIP3</title>
		<link>https://genomed.pt/sindrome-auto-inflamatoria-familiar-behcet-like-gene-tnfaip3/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 20 Apr 2022 22:03:05 +0000</pubDate>
				<category><![CDATA[Doenças do Sistema Imunitário]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF561]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=114196</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Síndrome auto-Inflamatória familiar, Behcet-like: gene TNFAIP3" data-especialidade-1="Doenças do Sistema Imunitário" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="#616744" data-num-genes="1" data-lista-genes="TNFAIP3" 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>

		</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/entry/616744' target='_blank' rel="noopener">#616744</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>						1					</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>						TNFAIP3					</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>Síndrome de Emberger: gene GATA2</title>
		<link>https://genomed.pt/sindrome-de-emberger-gene-gata2/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Thu, 21 Apr 2022 22:03:18 +0000</pubDate>
				<category><![CDATA[Doenças do Sistema Imunitário]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF562]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=114206</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Síndrome de Emberger: gene GATA2" data-especialidade-1="Doenças do Sistema Imunitário" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="#614038" data-num-genes="1" data-lista-genes="GATA2" 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>

		</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/entry/614038' target='_blank' rel="noopener">#614038</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>						1					</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>						GATA2					</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>Síndrome linfoproliferativa autoimune (ALPS): painel de genes por NGS</title>
		<link>https://genomed.pt/sindrome-linfoproliferativa-autoimune-alps-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 02:32:15 +0000</pubDate>
				<category><![CDATA[Doenças do Sistema Imunitário]]></category>
		<category><![CDATA[Imunodeficiências]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[Reumatologia]]></category>
		<category><![CDATA[PTDGF107]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20540</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Síndrome linfoproliferativa autoimune (ALPS): painel de genes por NGS" data-especialidade-1="Doenças do Sistema Imunitário" data-especialidade-2="Pediatria, Imunodeficiências, Reumatologia" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="19" data-lista-genes="ADA2, AICDA, CASP10, CASP8, CD40LG, CTLA4, FADD, FAS, FASLG, ITK, KRAS, LRBA, MAGT1, NRAS, PRKCD, RASGRP1, SH2D1A, STAT3, WAS" 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</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>						19					</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>						ADA2, AICDA, CASP10, CASP8, CD40LG, CTLA4, FADD, FAS, FASLG, ITK, KRAS, LRBA, MAGT1, NRAS, PRKCD, RASGRP1, SH2D1A, STAT3, WAS					</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>Via alterna do complemento / Síndrome hemolítico-urémica: painel de genes por NGS</title>
		<link>https://genomed.pt/via-alterna-do-complemento-sindrome-hemolitico-uremica-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 03:46:14 +0000</pubDate>
				<category><![CDATA[Doenças do Sistema Imunitário]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Reumatologia]]></category>
		<category><![CDATA[PTDGF109]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20872</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Via alterna do complemento / Síndrome hemolítico-urémica: painel de genes por NGS" data-especialidade-1="Doenças do Sistema Imunitário" data-especialidade-2="Reumatologia" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="12" data-lista-genes="ADAMTS13, C3, CD46, CFB, CFH, CFHR1, CFHR3, CFHR4, CFHR5, CFI, DGKE, MMACHC" 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</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>						12					</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>						ADAMTS13, C3, CD46, CFB, CFH, CFHR1, CFHR3, CFHR4, CFHR5, CFI, DGKE, MMACHC					</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>
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</rss>
