<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>NGS &#8211; GenoMed</title>
	<atom:link href="https://genomed.pt/category/nefrologia/ngs-nefrologia/feed/" rel="self" type="application/rss+xml" />
	<link>https://genomed.pt</link>
	<description>GenoMed</description>
	<lastBuildDate>Tue, 28 May 2024 22:02:23 +0000</lastBuildDate>
	<language>pt-PT</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=6.1.8</generator>

<image>
	<url>https://genomed.pt/wp-content/uploads/2020/06/cropped-favicon-genomed-32x32.png</url>
	<title>NGS &#8211; GenoMed</title>
	<link>https://genomed.pt</link>
	<width>32</width>
	<height>32</height>
</image> 
	<item>
		<title>Acidose tubular renal: genes ATP6V0A4, ATP6V1B1, SLC4A1</title>
		<link>https://genomed.pt/acidose-tubular-renal-genes-atp6v0a4-atp6v1b1-slc4a1/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:05:44 +0000</pubDate>
				<category><![CDATA[Nefrologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF244]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21332</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Acidose tubular renal: genes ATP6V0A4, ATP6V1B1, SLC4A1" data-especialidade-1="Nefrologia" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="3" data-lista-genes="ATP6V0A4, ATP6V1B1, SLC4A1" 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>Nefrologia</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>						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>						ATP6V0A4, ATP6V1B1, SLC4A1					</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>Cistinúria: genes SLC3A1, SLC7A9</title>
		<link>https://genomed.pt/cistinuria-genes-slc3a1-slc7a9/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:06:02 +0000</pubDate>
				<category><![CDATA[Nefrologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF246]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21340</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Cistinúria: genes SLC3A1, SLC7A9" data-especialidade-1="Nefrologia" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="2" data-lista-genes="SLC3A1, SLC7A9" 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>Nefrologia</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>						2					</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>						SLC3A1, SLC7A9					</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 renal crónica no jovem: painel de genes por NGS</title>
		<link>https://genomed.pt/doenca-renal-cronica-no-jovem-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 15 Mar 2023 23:02:45 +0000</pubDate>
				<category><![CDATA[Nefrologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF572]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=114460</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Doença renal crónica no jovem: painel de genes por NGS" data-especialidade-1="Nefrologia" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="" data-num-genes="85" data-lista-genes="ACE, ACTG2, ACTN4, AGT, AGTR1, AMN, ANKS6, ARHGDIA, C3, CD46, CEP164, CFB, CFH, CFHR5, CFI, CHD7, CHRM3, CLCN5, COL4A3, COL4A4, COL4A5, COQ2, COQ6, COQ8B, CTNS, CUBN, DGKE, DSTYK, EYA1, FAN1, FRAS1, FREM1, FREM2, GATA3, GLA, GLI3, GRIP1, HNF1B, HPSE2, INF2, INVS, ITGA3, ITGA8, LAMB2, LMX1B, LRIG2, MUC1, MYH9, MYO1E, NPHP1, NPHP3, NPHP4, NPHS1, NPHS2, NUP107, NUP93, OFD1, PAX2, PKD1, PKD2, PKHD1, PLCE1, REN, RPGRIP1L, RRM2B, SALL1, SARS2, SCARB2, SGPL1, SIX5, SMARCAL1, TBX18, TMEM67, TRAP1, TRIM8, TRPC6, TSC1, TSC2, TTC21B, UMOD, VHL, VIPAS39, VPS33B, WT1, XPNPEP3" 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>Nefrologia</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">
			
		</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>						85					</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>						ACE, ACTG2, ACTN4, AGT, AGTR1, AMN, ANKS6, ARHGDIA, C3, CD46, CEP164, CFB, CFH, CFHR5, CFI, CHD7, CHRM3, CLCN5, COL4A3, COL4A4, COL4A5, COQ2, COQ6, COQ8B, CTNS, CUBN, DGKE, DSTYK, EYA1, FAN1, FRAS1, FREM1, FREM2, GATA3, GLA, GLI3, GRIP1, HNF1B, HPSE2, INF2, INVS, ITGA3, ITGA8, LAMB2, LMX1B, LRIG2, MUC1, MYH9, MYO1E, NPHP1, NPHP3, NPHP4, NPHS1, NPHS2, NUP107, NUP93, OFD1, PAX2, PKD1, PKD2, PKHD1, PLCE1, REN, RPGRIP1L, RRM2B, SALL1, SARS2, SCARB2, SGPL1, SIX5, SMARCAL1, TBX18, TMEM67, TRAP1, TRIM8, TRPC6, TSC1, TSC2, TTC21B, UMOD, VHL, VIPAS39, VPS33B, WT1, XPNPEP3					</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 renal poliquística: painel de genes por NGS</title>
		<link>https://genomed.pt/doenca-renal-poliquistica-genes-pkd1-pkd2-pkhd1/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:07:14 +0000</pubDate>
				<category><![CDATA[Nefrologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF254]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21372</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Doença renal poliquística: painel de genes por NGS" data-especialidade-1="Nefrologia" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="6" data-lista-genes="DNAJB11, DZIP1L, GANAB, PKD1, PKD2, PKHD1" 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>Nefrologia</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>						6					</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>						DNAJB11, DZIP1L, GANAB, PKD1, PKD2, PKHD1					</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 renal poliquística: painel de genes por NGS (painel alargado)</title>
		<link>https://genomed.pt/doenca-renal-poliquistica-painel-de-genes-por-ngs-painel-alargado/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:07:22 +0000</pubDate>
				<category><![CDATA[Nefrologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF255]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21376</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Doença renal poliquística: painel de genes por NGS (painel alargado)" data-especialidade-1="Nefrologia" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="32" data-lista-genes="ABCC8, ALG8, BICC1, BLK, COL4A1, DNAJB11, DZIP1L, GANAB, GCK, HNF1B, HNF4A, INS, INVS, KCNJ11, KLF11, LRP5, NEUROD1, NOTCH2, NPHP3, OFD1, PAX4, PDX1, PKD1, PKD2, PKHD1, PRKCSH, SEC61B, SEC63, TSC1, TSC2, UMOD, VHL" 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>Nefrologia</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>						32					</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>						ABCC8, ALG8, BICC1, BLK, COL4A1, DNAJB11, DZIP1L, GANAB, GCK, HNF1B, HNF4A, INS, INVS, KCNJ11, KLF11, LRP5, NEUROD1, NOTCH2, NPHP3, OFD1, PAX4, PDX1, PKD1, PKD2, PKHD1, PRKCSH, SEC61B, SEC63, TSC1, TSC2, UMOD, VHL					</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>Glicosúria renal familiar: gene SLC2A2, SLC5A2</title>
		<link>https://genomed.pt/glicosuria-renal-familiar-gene-slc2a2-slc5a2/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:08:07 +0000</pubDate>
				<category><![CDATA[Nefrologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF260]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21396</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Glicosúria renal familiar: gene SLC2A2, SLC5A2" data-especialidade-1="Nefrologia" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="2" data-lista-genes="SLC2A2, SLC5A2" 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>Nefrologia</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>						2					</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>						SLC2A2, SLC5A2					</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>Hiperoxalúria primária: genes AGXT, GRHPR, HOGA1</title>
		<link>https://genomed.pt/hiperoxaluria-primaria-genes-agxt-grhpr-hoga1/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Sat, 15 Jan 2022 23:05:26 +0000</pubDate>
				<category><![CDATA[Nefrologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF557]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=113628</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Hiperoxalúria primária: genes AGXT, GRHPR, HOGA1" data-especialidade-1="Nefrologia" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="3" data-lista-genes="AGXT, GRHPR, HOGA1" 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>Nefrologia</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>						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>						AGXT, GRHPR, HOGA1					</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>Hipertensão arterial: painel de genes por NGS</title>
		<link>https://genomed.pt/hipertensao-monogenica-painel-de-genes-por-ngs-2/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Sat, 15 Aug 2020 00:02:26 +0000</pubDate>
				<category><![CDATA[Cardiologia]]></category>
		<category><![CDATA[Cardiologia Pediátrica]]></category>
		<category><![CDATA[Endocrinologia]]></category>
		<category><![CDATA[Medicina Interna]]></category>
		<category><![CDATA[Nefrologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF8]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=22513</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Hipertensão arterial: painel de genes por NGS" data-especialidade-1="Cardiologia" data-especialidade-2="Cardiologia Pediátrica, Nefrologia, Medicina Interna, Endocrinologia" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="27" data-lista-genes="AOC1, ASIC3, CLCNKB, CUL3, CYP11B1, CYP11B2, CYP17A1, HSD11B2, KCNH2, KCNJ1, KLHL3, NOS3, NR3C2, PDE3A, RET, SDHA, SDHAF2, SDHB, SDHC, SDHD, SLC12A1, SLC12A3, SCNN1B, SCNN1G, VHL, WNK1, WNK4" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Cardiologia</p>
<p> Cardiologia Pediátrica, Nefrologia, Medicina Interna, Endocrinologia</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>						27					</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>						AOC1, ASIC3, CLCNKB, CUL3, CYP11B1, CYP11B2, CYP17A1, HSD11B2, KCNH2, KCNJ1, KLHL3, NOS3, NR3C2, PDE3A, RET, SDHA, SDHAF2, SDHB, SDHC, SDHD, SLC12A1, SLC12A3, SCNN1B, SCNN1G, VHL, WNK1, WNK4					</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>Hipertensão pulmonar hereditária: painel de genes por NGS</title>
		<link>https://genomed.pt/hipertensao-arterial-pulmonar-hereditaria-painel-de-genes-por-ngs-2/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Sat, 15 Aug 2020 00:02:19 +0000</pubDate>
				<category><![CDATA[Cardiologia]]></category>
		<category><![CDATA[Medicina Interna]]></category>
		<category><![CDATA[Nefrologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[Pneumologia]]></category>
		<category><![CDATA[PTDGF7]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=22509</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Hipertensão pulmonar hereditária: painel de genes por NGS" data-especialidade-1="Cardiologia" data-especialidade-2="Nefrologia, Pneumologia, Medicina Interna" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="15" data-lista-genes="ABCC8, BMPR2, ACVRL1, ATP13A3, CAV1, EIF2AK4, ENG, GDF2, GGCX, KCNK3, KDR, SMAD9, SOX17, TBX4, TET2" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Cardiologia</p>
<p> Nefrologia, Pneumologia, 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>						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>						ABCC8, BMPR2, ACVRL1, ATP13A3, CAV1, EIF2AK4, ENG, GDF2, GGCX, KCNK3, KDR, SMAD9, SOX17, TBX4, TET2					</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>Litíase renal: painel de genes por NGS</title>
		<link>https://genomed.pt/litiase-renal-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 18 May 2022 22:06:08 +0000</pubDate>
				<category><![CDATA[Nefrologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF565]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=114256</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Litíase renal: painel de genes por NGS" data-especialidade-1="Nefrologia" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="" data-num-genes="30" data-lista-genes="ADCY10, AGXT, AP2S1, APRT, ATP6V0A4, ATP6V1B1, CA2, CASR, CLCN5, CLDN16, CLDN19, CYP24A1, FAM20A, GNA11, GRHPR, HNF4A, HOGA1, HPRT1, KCNJ1, OCRL, SLC12A1, SLC22A12, SLC26A1, SLC2A9, SLC34A1, SLC34A3, SLC3A1, SLC4A1, SLC7A9, SLC9A3R1" 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>Nefrologia</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">
			
		</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>						30					</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>						ADCY10, AGXT, AP2S1, APRT, ATP6V0A4, ATP6V1B1, CA2, CASR, CLCN5, CLDN16, CLDN19, CYP24A1, FAM20A, GNA11, GRHPR, HNF4A, HOGA1, HPRT1, KCNJ1, OCRL, SLC12A1, SLC22A12, SLC26A1, SLC2A9, SLC34A1, SLC34A3, SLC3A1, SLC4A1, SLC7A9, SLC9A3R1					</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>
