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	<title>NGS &#8211; GenoMed</title>
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	<title>NGS &#8211; GenoMed</title>
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	<item>
		<title>Artrogripose distal: painel de genes por NGS</title>
		<link>https://genomed.pt/artrogripose-distal-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:41:54 +0000</pubDate>
				<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[PTDGF483]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=22264</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Artrogripose distal: painel de genes por NGS" data-especialidade-1="Pediatria" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="9" data-lista-genes="ECEL1, FBN2, MYBPC1, MYH3, MYH8, PIEZO2, TPM2, TNNI2, TNNT3" 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>Pediatria</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>						9					</p>

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				</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>						ECEL1, FBN2, MYBPC1, MYH3, MYH8, PIEZO2, TPM2, TNNI2, TNNT3					</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>Craniossinostoses: painel de genes por NGS</title>
		<link>https://genomed.pt/craniossinostoses-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:42:11 +0000</pubDate>
				<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[PTDGF485]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=22272</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Craniossinostoses: painel de genes por NGS" data-especialidade-1="Pediatria" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="42" data-lista-genes="ALPL, ALX3, ALX4, BMP4, EDN3, EDNRB, EFNB1, ERF, ESCO2, FGFR1, FGFR2, FGFR3, FLNB, FREM1, GDF5, GLI3, IFT122, IFT140, IL11RA, IMPAD1, IRX5, MASP1, MEGF8, MITF, MSX2, NOG, PAX3, POR, RAB23, RECQL4, RET, SCARF2, SKI, SOX10, TCF12, TGFBR1, TGFBR2, TMCO1, TTR, TWIST1, WDR19, WDR35" 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>Pediatria</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>						42					</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>						ALPL, ALX3, ALX4, BMP4, EDN3, EDNRB, EFNB1, ERF, ESCO2, FGFR1, FGFR2, FGFR3, FLNB, FREM1, GDF5, GLI3, IFT122, IFT140, IL11RA, IMPAD1, IRX5, MASP1, MEGF8, MITF, MSX2, NOG, PAX3, POR, RAB23, RECQL4, RET, SCARF2, SKI, SOX10, TCF12, TGFBR1, TGFBR2, TMCO1, TTR, TWIST1, WDR19, WDR35					</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>Défice de surfactante: painel de genes por NGS</title>
		<link>https://genomed.pt/defice-de-surfactante-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 03:17:16 +0000</pubDate>
				<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[Pneumologia]]></category>
		<category><![CDATA[PTDGF525]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20648</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Défice de surfactante: painel de genes por NGS" data-especialidade-1="Pneumologia" data-especialidade-2="Pediatria" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="PS265120" data-num-genes="7" data-lista-genes="ABCA3, CSF2RA, CSF2RB, SFTPA1, SFTPB, SFTPC, SFTPD" 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>Pneumologia</p>
<p> Pediatria</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/PS265120' target='_blank' rel="noopener">PS265120</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>						7					</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>						ABCA3, CSF2RA, CSF2RB, SFTPA1, SFTPB, SFTPC, SFTPD					</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>Displasia epifisária múltipla: painel de genes por NGS</title>
		<link>https://genomed.pt/displasia-epifisaria-multipla-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:42:29 +0000</pubDate>
				<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[PTDGF487]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=22280</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Displasia epifisária múltipla: painel de genes por NGS" data-especialidade-1="Pediatria" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="8" data-lista-genes="COL2A1, COL9A1, COL9A2, COL9A3, COMP, MATN3, SLC26A2, UFSP2" 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>Pediatria</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>						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>						COL2A1, COL9A1, COL9A2, COL9A3, COMP, MATN3, SLC26A2, UFSP2					</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>Displasias esqueléticas: painel de genes por NGS</title>
		<link>https://genomed.pt/displasias-esqueleticas-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:42:56 +0000</pubDate>
				<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[PTDGF490]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=22292</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Displasias esqueléticas: painel de genes por NGS" data-especialidade-1="Pediatria" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="106" data-lista-genes="ACP5, ADAMTS10, ADAMTSL2, AGPS, ALPL, ANKH, ARSE, B3GALT6, BMP1, BMPR1B, CA2, CANT1, CDC6, CDKN1C, CDT1, CHST3, CLCN7, COL10A1, COL11A1, COL11A2, COL1A1, COL1A2, COL2A1, COL9A1, COL9A2, COL9A3, COMP, CRTAP, CSPP1, CTSK, CUL7, CYP27B1, DHCR24, DLL3, DVL1, DYM, DYNC2H1, EBP, EIF2AK3, EMILIN1, ENPP1, ESCO2, EVC, EVC2, FAM20C, FGF23, FGFR1, FGFR2, FGFR3, FKBP10, FLNA, FLNB, GDF5, GNPAT, HSPG2, IFT140, IFT172, IFT80, IHH, IKBKG, KAT6B, LBR, LIFR, LMX1B, LRP5, LTBP2, MATN3, MMP9, NEK1, NPR2, OBSL1, ORC1, ORC4, ORC6, P3H1, PAPSS2, PCNT, PEX7, PHEX, PLOD2, PPIB, PTH1R, ROR2, RUNX2, SBDS, SERPINF1, SERPINH1, SHOX, SLC26A2, SLC34A3, SLC39A13, SMAD4, SMARCAL1, SOX9, TCIRG1, TGFB1, TNFRSF11A, TNFRSF11B, TRAPPC2, TRPV4, TTC21B, VDR, WDR19, WDR35, WISP3, WNT5A" 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>Pediatria</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>						106					</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>						ACP5, ADAMTS10, ADAMTSL2, AGPS, ALPL, ANKH, ARSE, B3GALT6, BMP1, BMPR1B, CA2, CANT1, CDC6, CDKN1C, CDT1, CHST3, CLCN7, COL10A1, COL11A1, COL11A2, COL1A1, COL1A2, COL2A1, COL9A1, COL9A2, COL9A3, COMP, CRTAP, CSPP1, CTSK, CUL7, CYP27B1, DHCR24, DLL3, DVL1, DYM, DYNC2H1, EBP, EIF2AK3, EMILIN1, ENPP1, ESCO2, EVC, EVC2, FAM20C, FGF23, FGFR1, FGFR2, FGFR3, FKBP10, FLNA, FLNB, GDF5, GNPAT, HSPG2, IFT140, IFT172, IFT80, IHH, IKBKG, KAT6B, LBR, LIFR, LMX1B, LRP5, LTBP2, MATN3, MMP9, NEK1, NPR2, OBSL1, ORC1, ORC4, ORC6, P3H1, PAPSS2, PCNT, PEX7, PHEX, PLOD2, PPIB, PTH1R, ROR2, RUNX2, SBDS, SERPINF1, SERPINH1, SHOX, SLC26A2, SLC34A3, SLC39A13, SMAD4, SMARCAL1, SOX9, TCIRG1, TGFB1, TNFRSF11A, TNFRSF11B, TRAPPC2, TRPV4, TTC21B, VDR, WDR19, WDR35, WISP3, WNT5A					</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 de Moyamoya: genes ACTA2, GUCY1A3, RNF213</title>
		<link>https://genomed.pt/doenca-de-moyamoya-genes-acta2-gucy1a3-rnf213/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Fri, 14 Jan 2022 23:04:54 +0000</pubDate>
				<category><![CDATA[Neurologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[PTDGF553]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=113608</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Doença de Moyamoya: genes ACTA2, GUCY1A3, RNF213" data-especialidade-1="Neurologia" data-especialidade-2="Pediatria" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="PS252350" data-num-genes="3" data-lista-genes="ACTA2, GUCY1A3, RNF213" 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>Neurologia</p>
<p> Pediatria</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/PS252350' target='_blank' rel="noopener">PS252350</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>						3					</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>						ACTA2, GUCY1A3, RNF213					</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>Doença pulmonar: painel de genes por NGS (painel alargado)</title>
		<link>https://genomed.pt/doenca-pulmonar-painel-de-genes-por-ngs-painel-alargado/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 03:17:31 +0000</pubDate>
				<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[Pneumologia]]></category>
		<category><![CDATA[PTDGF527]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20652</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Doença pulmonar: painel de genes por NGS (painel alargado)" data-especialidade-1="Pneumologia" data-especialidade-2="Pediatria" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="67" data-lista-genes="ABCA3, CCDC39, CCDC40, CFTR, CHAT, CHRNA1, CHRNB1, CHRND, CHRNE, COLQ, CSF2RA, CSF2RB, DKC1, DNAAF1, DNAAF2, DNAH1, DNAH11, DNAH5, DNAI1, DNAI2, DNAL1, EDN3, EFEMP2, ELMOD2, ELN, FBLN5, FLCN, FOXF1, GAS8, GLRA1, HPS1, HPS4, ITGA3, LTBP4, MECP2, NAF1, NF1, NKX2-1, NME8, PARN, PHOX2B, PIH1D3, RAPSN, RET, RSPH3, RSPH4A, RSPH9, RTEL1, SCN4A, SCNN1A, SCNN1B, SERPINA1, SFTPA1, SFTPA2, SFTPB, SFTPC, SLC34A2, SLC6A5, SLC7A7, SMPD1, STAT3, TERC, TERT, TINF2, TSC1, TSC2, ZEB2" 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>Pneumologia</p>
<p> Pediatria</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>						67					</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>						ABCA3, CCDC39, CCDC40, CFTR, CHAT, CHRNA1, CHRNB1, CHRND, CHRNE, COLQ, CSF2RA, CSF2RB, DKC1, DNAAF1, DNAAF2, DNAH1, DNAH11, DNAH5, DNAI1, DNAI2, DNAL1, EDN3, EFEMP2, ELMOD2, ELN, FBLN5, FLCN, FOXF1, GAS8, GLRA1, HPS1, HPS4, ITGA3, LTBP4, MECP2, NAF1, NF1, NKX2-1, NME8, PARN, PHOX2B, PIH1D3, RAPSN, RET, RSPH3, RSPH4A, RSPH9, RTEL1, SCN4A, SCNN1A, SCNN1B, SERPINA1, SFTPA1, SFTPA2, SFTPB, SFTPC, SLC34A2, SLC6A5, SLC7A7, SMPD1, STAT3, TERC, TERT, TINF2, TSC1, TSC2, ZEB2					</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 respiratória do recém-nascido: painel de genes por NGS</title>
		<link>https://genomed.pt/doenca-respiratoria-do-recem-nascido-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 03:17:40 +0000</pubDate>
				<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pediatria]]></category>
		<category><![CDATA[Pneumologia]]></category>
		<category><![CDATA[PTDGF528]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=20656</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Doença respiratória do recém-nascido: painel de genes por NGS" data-especialidade-1="Pneumologia" data-especialidade-2="Pediatria" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="56" data-lista-genes="ABCA3, ARMC4, C21orf59, CCDC103, CCDC114, CCDC151, CCDC39, CCDC40, CCDC65, CCNO, CFTR, COPA, CSF2RA, CSF2RB, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH1, DNAH11, DNAH5, DNAH8, DNAH9, DNAI1, DNAI2, DNAJB13, DNAL1, DRC1, FGFR2, FLNA, FOXF1, GAS2L2, GAS8, HYDIN, INVS, LRRC6, MCIDAS, NKX2-1, NME8, OFD1, PIH1D3, RPGR, RSPH1, RSPH3, RSPH4A, RSPH9, SFTPA1, SFTPB, SFTPC, SFTPD, SPAG1, TBX4, TMEM173, TTC25, ZMYND10" 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>Pneumologia</p>
<p> Pediatria</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>						56					</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>						ABCA3, ARMC4, C21orf59, CCDC103, CCDC114, CCDC151, CCDC39, CCDC40, CCDC65, CCNO, CFTR, COPA, CSF2RA, CSF2RB, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH1, DNAH11, DNAH5, DNAH8, DNAH9, DNAI1, DNAI2, DNAJB13, DNAL1, DRC1, FGFR2, FLNA, FOXF1, GAS2L2, GAS8, HYDIN, INVS, LRRC6, MCIDAS, NKX2-1, NME8, OFD1, PIH1D3, RPGR, RSPH1, RSPH3, RSPH4A, RSPH9, SFTPA1, SFTPB, SFTPC, SFTPD, SPAG1, TBX4, TMEM173, TTC25, ZMYND10					</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>
	</channel>
</rss>
