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	<title>Neurologia &#8211; GenoMed</title>
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	<title>Neurologia &#8211; GenoMed</title>
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	<item>
		<title>Amiotrofia neurálgica hereditária: gene SEPTIN9</title>
		<link>https://genomed.pt/amiotrofia-neuralgica-hereditaria-gene-septin9/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:12:36 +0000</pubDate>
				<category><![CDATA[Neurologia]]></category>
		<category><![CDATA[Outras metodologias]]></category>
		<category><![CDATA[PTDGF290]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21516</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Amiotrofia neurálgica hereditária: gene SEPTIN9" data-especialidade-1="Neurologia" data-especialidade-2="" data-metodologia="Sequenciação" data-codigo-sns="34900" data-omim="#162100" data-num-genes="1" data-lista-genes="SEPTIN9" data-tat="4 a 6 semanas" 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>

		</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>						Sequenciação					</p>

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

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						<a href='https://www.omim.org/entry/162100' target='_blank' rel="noopener">#162100</a>					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						1					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						SEPTIN9					</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>						4 a 6 semanas					</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>Angiopatia amiloide familiar: painel de genes por NGS</title>
		<link>https://genomed.pt/angiopatia-amiloide-familiar-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:12:45 +0000</pubDate>
				<category><![CDATA[Neurologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF291]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21520</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Angiopatia amiloide familiar: painel de genes por NGS" data-especialidade-1="Neurologia" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="27" data-lista-genes="APOE (alelo e4), APP, CHCHD10, CHMP2B, COL4A1, COL4A2, CSF1R, CST3, CTC1, DCTN1, ITM2B, GLA, GRN, GSN, HTR1A, MAPT, NOTCH3, PRNP, PSEN1, PSEN2, SNCA, SNCB, SQSTM1, TARDBP, TBK1, TREX1, TTR" data-tat="2 a 3 meses" data-tipo-amostra="Sangue periférico em EDTA (3 a 6mL); estável 48h à temperatura ambiente (TA) ou 72h refrigerado 
 ou 
 ADN (>5μg com concentração >20ng/μL); estável 48h à TA ou >48h refrigerado<br />
 &#8211;<br />
 Para outros tipos de amostra, por favor contacte o laboratório.&#8221; data-req-name=&#8221;https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf&#8221;/>	<div class="vc_row wpb_row vc_row-fluid" >		<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">			<div class="vc_separator wpb_content_element vc_separator_align_center vc_sep_width_100 vc_sep_border_width_3 vc_sep_pos_align_center vc_separator_no_text" ><span class="vc_sep_holder vc_sep_holder_l"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span><span class="vc_sep_holder vc_sep_holder_r"><span  style="border-color:#43d4cb;" class="vc_sep_line"></span></span>
</div>			<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>						<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591203652363" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Especialidade(s) / Outra(s) Especialidade(s)</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591266754832" >
		<div class="wpb_wrapper">
			
<p>Neurologia</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>						APOE (alelo e4), APP, CHCHD10, CHMP2B, COL4A1, COL4A2, CSF1R, CST3, CTC1, DCTN1, ITM2B, GLA, GRN, GSN, HTR1A, MAPT, NOTCH3, PRNP, PSEN1, PSEN2, SNCA, SNCB, SQSTM1, TARDBP, TBK1, TREX1, TTR					</p>

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

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

		</div>
	</div>
					<div class="vc_empty_space"   style="height: 30px"><span class="vc_empty_space_inner"></span></div>				</div></div></div>			</div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591277235133 mkdf-content-aligment-left" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<a itemprop="url" href="https://genomed.pt/wp-content/uploads/2020/07/REQUISICAO_DOENCAS_GENETICAS.pdf" target="_blank"  class="mkdf-btn mkdf-btn-medium mkdf-btn-solid mkdf-btn-solid-dark mkdf-btn-icon"  >
    <span class="mkdf-btn-text">Requisitar</span>
    <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>Ataxia com deficiência em vitamina E: gene TTPA</title>
		<link>https://genomed.pt/ataxia-com-deficiencia-em-vitamina-e-gene-ttpa/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:12:53 +0000</pubDate>
				<category><![CDATA[Neurologia]]></category>
		<category><![CDATA[Outras metodologias]]></category>
		<category><![CDATA[PTDGF292]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21524</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Ataxia com deficiência em vitamina E: gene TTPA" data-especialidade-1="Neurologia" data-especialidade-2="" data-metodologia="Sequenciação" data-codigo-sns="34900" data-omim="#277460" data-num-genes="1" data-lista-genes="TTPA" data-tat="4 a 6 semanas" 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>

		</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>						Sequenciação					</p>

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

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						<a href='https://www.omim.org/entry/277460' target='_blank' rel="noopener">#277460</a>					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						1					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						TTPA					</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>						4 a 6 semanas					</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>Ataxia de Friedreich: gene FXN</title>
		<link>https://genomed.pt/ataxia-de-friedreich-gene-fxn/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:13:02 +0000</pubDate>
				<category><![CDATA[Neurologia]]></category>
		<category><![CDATA[Outras metodologias]]></category>
		<category><![CDATA[PTDGF293]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21528</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Ataxia de Friedreich: gene FXN" data-especialidade-1="Neurologia" data-especialidade-2="" data-metodologia="Análise de Fragmentos" data-codigo-sns="34900" data-omim="#229300" data-num-genes="1" data-lista-genes="FXN" data-tat="8 a 10 semanas" 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>

		</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>						Análise de Fragmentos					</p>

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

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						<a href='https://www.omim.org/entry/229300' target='_blank' rel="noopener">#229300</a>					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						1					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						FXN					</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>						8 a 10 semanas					</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>Ataxia episódica tipo 2: gene CACNA1A</title>
		<link>https://genomed.pt/ataxia-episodica-tipo-2-gene-cacna1a/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:13:11 +0000</pubDate>
				<category><![CDATA[Neurologia]]></category>
		<category><![CDATA[Outras metodologias]]></category>
		<category><![CDATA[PTDGF294]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21532</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Ataxia episódica tipo 2: gene CACNA1A" data-especialidade-1="Neurologia" data-especialidade-2="" data-metodologia="Sequenciação" data-codigo-sns="34900" data-omim="#108500" data-num-genes="1" data-lista-genes="CACNA1A" 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>

		</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>						Sequenciação					</p>

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

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >OMIM</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204459457" >
		<div class="wpb_wrapper">
			<p>						<a href='https://www.omim.org/entry/108500' target='_blank' rel="noopener">#108500</a>					</p>

		</div>
	</div>
				</div></div></div>				<div class="wpb_column vc_column_container vc_col-sm-3"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Nº de Genes</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204224415" >
		<div class="wpb_wrapper">
			<p>						1					</p>

		</div>
	</div>
				</div></div></div>			</div>			<div class="vc_empty_space"   style="height: 20px"><span class="vc_empty_space_inner"></span></div>			<div class="vc_row wpb_row vc_inner vc_row-fluid vc_custom_1591204729039" >				<div class="wpb_column vc_column_container vc_col-sm-12"><div class="vc_column-inner"><div class="wpb_wrapper">					<h6 style="text-align: left" class="vc_custom_heading" >Lista de Genes / Mutações</h6>					
	<div class="wpb_text_column wpb_content_element  vc_custom_1591204819491" >
		<div class="wpb_wrapper">
			<p>						CACNA1A					</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>Ataxias espinocerebelosas: SCA1, 2, 3, 6, 7, 8 e 12</title>
		<link>https://genomed.pt/ataxias-espinocerebelosas-sca1-2-3-6-7-8-e-12/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:13:29 +0000</pubDate>
				<category><![CDATA[Neurologia]]></category>
		<category><![CDATA[Outras metodologias]]></category>
		<category><![CDATA[PTDGF296]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21540</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Ataxias espinocerebelosas: SCA1, 2, 3, 6, 7, 8 e 12" data-especialidade-1="Neurologia" data-especialidade-2="" data-metodologia="Análise de Fragmentos" data-codigo-sns="34900" data-omim="-" data-num-genes="7" data-lista-genes="SCA1, SCA2, SCA3, SCA6, SCA7, SCA8, SCA12" data-tat="8 a 10 semanas" 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>

		</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>						Análise de Fragmentos					</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>						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>						SCA1, SCA2, SCA3, SCA6, SCA7, SCA8, SCA12					</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>						8 a 10 semanas					</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>Ataxias recessivas: painel de genes por NGS</title>
		<link>https://genomed.pt/ataxias-recessivas-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:13:37 +0000</pubDate>
				<category><![CDATA[Neurologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF297]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21544</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Ataxias recessivas: painel de genes por NGS" data-especialidade-1="Neurologia" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="17" data-lista-genes="AFG3L2, ANO10, ATM, COQ8A, MRE11, MTPAP, MTTP, PIK3R5, POLG, SACS, SETX, SIL1, SPTBN2, SYNE1, SYT14, TDP1, ZNF592" 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>

		</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>						17					</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>						AFG3L2, ANO10, ATM, COQ8A, MRE11, MTPAP, MTTP, PIK3R5, POLG, SACS, SETX, SIL1, SPTBN2, SYNE1, SYT14, TDP1, ZNF592					</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>Ataxias: painel de genes por NGS (painel alargado)</title>
		<link>https://genomed.pt/ataxias-painel-de-genes-por-ngs-painel-alargado/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:13:20 +0000</pubDate>
				<category><![CDATA[Neurologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF295]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21536</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Ataxias: painel de genes por NGS (painel alargado)" data-especialidade-1="Neurologia" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="433" data-lista-genes="AAAS, AARS, ABCA2, ABCB7, ABHD12, ACBD6, ACO2, ADCY5, ADGRG1, ADPRHL2, AFG3L2, AGTPBP1, AHI1, ALDH5A1, ALG1, ALG11, ALG12, ALG14, ALG3, ALG6, ALG8, ALG9, AMPD2, ANO10, AP1S2, APTX, ARL13B, ARL3, ARMC9, ARSA, ASL, ATAD3A, ATCAY, ATG7, ATM, ATP1A2, ATP1A3, ATP2B3, ATP6AP1, ATP6V0A1, ATP6V0A2, ATP7B, ATP8A2, AUH, B3GALNT2, B3GALT6, B3GAT3, B3GLCT, B4GALNT1, B4GALT1, B4GALT7, B4GAT1, B9D2, BBS1, BRF1, C2CD3, C5orf42, CA8, CACNA1A, CACNA1G, CACNA2D2, CAD, CAMTA1, CAPN1, CAPRIN1, CASK, CBY1, CC2D2A, CCDC115, CENPF, CEP104, CEP290, CEP41, CHMP1A, CHP1, CHST14, CHST3, CHST6, CHSY1, CLCN2, CLN5, CLN6, CLP1, CLPP, COA7, COASY, COG1, COG3, COG4, COG5, COG6, COG7, COG8, COQ4, COQ8A, COX20, CP, CRB2, CSGALNACT1, CSPP1, CSTB, CTBP1, CWF19L1, CYP27A1, CYP2U1, DAG1, DAGLA, DARS2, DCC, DDHD2, DDOST, DDX59, DHCR7, DHDDS, DHRSX, DKC1, DLG4, DNAJC19, DNAJC3, DNAJC5, DNMT1, DOCK3, DOLK, DPAGT1, DPM1, DPM2, DPM3, DPYSL5, DYNC1H1, EBF3, EDEM3, EEF2, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, ELOVL4, ELOVL5, EN1, EOGT, EPM2A, ERCC4, EVC, EVC2, EXOC3L2, EXOSC3, EXOSC5, EXOSC8, EXOSC9, EXT1, EXT2, FA2H, FAM149B1, FBXL4, FDXR, FEM1C, FGF14, FKRP, FKTN, FLVCR1, FOLR1, FRMD5, FUK, FUT8, FXN, G6PC3, GALC, GALNT2, GALNT3, GBA2, GDAP2, GEMIN5, GFAP, GFPT1, GJC2, GLI3, GLRA1, GLRB, GLS, GMPPA, GMPPB, GNE, GORAB, GOSR2, GPAA1, GRID2, GRM1, GRN, HARS, HEATR5B, HEXA, HEXB, HMBS, HYLS1, ICK, IFT74, INPP5E, INTS11, IRF2BPL, ISPD, ITPR1, KCNA1, KCNA2, KCNC3, KCND3, KCNJ10, KCNN2, KCNQ2, KCNQ3, KIAA0586, KIAA0753, KIF1A, KIF1C, KIF7, LAMA1, LARGE1, LARS2, LETM1, LFNG, LIG3, LNPK, MAG, MAGT1, MAN1B1, MAN2B2, MAPK8IP3, MARS2, MFN2, MGAT2, MINPP1, MKS1, MMACHC, MOGS, MORC2, MPDU1, MPI, MRE11, MSTO1, MT-ATP6, MTCL1, MTFMT, MTPAP, MTTP, MVK, NAA60, NAXE, NFASC, NGLY1, NHLRC1, NKX2-1, NKX6-2, NPC1, NPC2, NPHP1, NPHP3, NPTX1, OFD1, OGDHL, OPA1, OPA3, OPHN1, PACS2, PAX6, PDYN, PEX16, PEX2, PEX6, PGAP2, PGAP3, PGM1, PGM3, PHGDH, PI4KA, PIBF1, PIGA, PIGL, PIGM, PIGN, PIGO, PIGS, PIGT, PIGV, PIGW, PITRM1, PLA2G6, PMM2, PMPCA, PMPCB, PNKD, PNKP, PNPLA6, PNPT1, POC1B, POLG, POLR3A, POLR3B, POLR3K, POMGNT1, POMGNT2, POMK, POMT1, POMT2, POU4F1, PRDM13, PRDX3, PRKCG, PRNP, PRPS1, PRRT2, PTF1A, PTRH2, PUM1, RARS2, RELN, RFT1, RFXANK, RNF170, RNF216, RNF220, ROBO3, RORA, RPGRIP1L, SACS, SAMD9L, SAR1B, SCLT1, SCN1A, SCN2A, SCN8A, SCYL1, SEC23B, SEPSECS, SETX, SIL1, SLC17A5, SLC1A3, SLC25A46, SLC2A1, SLC35A1, SLC35A2, SLC35C1, SLC35D1, SLC37A4, SLC39A8, SLC44A1, SLC52A2, SLC9A1, SLC9A6, SMPD4, SNAP25, SNX14, SPG7, SPR, SPTAN1, SPTBN2, SQSTM1, SRD5A3, SSR3, SSR4, ST3GAL3, ST3GAL5, STT3A, STUB1, SUFU, SVBP, SYNE1, SYNGAP1, TANGO2, TBC1D23, TCTN1, TCTN2, TCTN3, TDP1, TDP2, TECPR2, TERT, TGM6, THG1L, TINF2, TMEM106B, TMEM107, TMEM138, TMEM165, TMEM199, TMEM216, TMEM218, TMEM231, TMEM237, TMEM240, TMEM5, TMEM67, TOE1, TOGARAM1, TPP1, TRAPPC11, TSEN15, TSEN2, TSEN34, TSEN54, TTBK2, TTC19, TTPA, TUBA1A, TUBA4A, TUBA8, TUBB2B, TUBB3, TUBB4A, TUSC3, TWNK, TXNDC15, UBA5, UBTF, UCHL1, VAMP1, VLDLR, VPS13B, VPS13D, VPS41, VPS53, VRK1, WDR73, WDR81, WFS1, WWOX, XRCC1, XYLT1, XYLT2, ZFHX3, ZFYVE26, ZNF423, ZSWIM6" 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>

		</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>						433					</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>						AAAS, AARS, ABCA2, ABCB7, ABHD12, ACBD6, ACO2, ADCY5, ADGRG1, ADPRHL2, AFG3L2, AGTPBP1, AHI1, ALDH5A1, ALG1, ALG11, ALG12, ALG14, ALG3, ALG6, ALG8, ALG9, AMPD2, ANO10, AP1S2, APTX, ARL13B, ARL3, ARMC9, ARSA, ASL, ATAD3A, ATCAY, ATG7, ATM, ATP1A2, ATP1A3, ATP2B3, ATP6AP1, ATP6V0A1, ATP6V0A2, ATP7B, ATP8A2, AUH, B3GALNT2, B3GALT6, B3GAT3, B3GLCT, B4GALNT1, B4GALT1, B4GALT7, B4GAT1, B9D2, BBS1, BRF1, C2CD3, C5orf42, CA8, CACNA1A, CACNA1G, CACNA2D2, CAD, CAMTA1, CAPN1, CAPRIN1, CASK, CBY1, CC2D2A, CCDC115, CENPF, CEP104, CEP290, CEP41, CHMP1A, CHP1, CHST14, CHST3, CHST6, CHSY1, CLCN2, CLN5, CLN6, CLP1, CLPP, COA7, COASY, COG1, COG3, COG4, COG5, COG6, COG7, COG8, COQ4, COQ8A, COX20, CP, CRB2, CSGALNACT1, CSPP1, CSTB, CTBP1, CWF19L1, CYP27A1, CYP2U1, DAG1, DAGLA, DARS2, DCC, DDHD2, DDOST, DDX59, DHCR7, DHDDS, DHRSX, DKC1, DLG4, DNAJC19, DNAJC3, DNAJC5, DNMT1, DOCK3, DOLK, DPAGT1, DPM1, DPM2, DPM3, DPYSL5, DYNC1H1, EBF3, EDEM3, EEF2, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, ELOVL4, ELOVL5, EN1, EOGT, EPM2A, ERCC4, EVC, EVC2, EXOC3L2, EXOSC3, EXOSC5, EXOSC8, EXOSC9, EXT1, EXT2, FA2H, FAM149B1, FBXL4, FDXR, FEM1C, FGF14, FKRP, FKTN, FLVCR1, FOLR1, FRMD5, FUK, FUT8, FXN, G6PC3, GALC, GALNT2, GALNT3, GBA2, GDAP2, GEMIN5, GFAP, GFPT1, GJC2, GLI3, GLRA1, GLRB, GLS, GMPPA, GMPPB, GNE, GORAB, GOSR2, GPAA1, GRID2, GRM1, GRN, HARS, HEATR5B, HEXA, HEXB, HMBS, HYLS1, ICK, IFT74, INPP5E, INTS11, IRF2BPL, ISPD, ITPR1, KCNA1, KCNA2, KCNC3, KCND3, KCNJ10, KCNN2, KCNQ2, KCNQ3, KIAA0586, KIAA0753, KIF1A, KIF1C, KIF7, LAMA1, LARGE1, LARS2, LETM1, LFNG, LIG3, LNPK, MAG, MAGT1, MAN1B1, MAN2B2, MAPK8IP3, MARS2, MFN2, MGAT2, MINPP1, MKS1, MMACHC, MOGS, MORC2, MPDU1, MPI, MRE11, MSTO1, MT-ATP6, MTCL1, MTFMT, MTPAP, MTTP, MVK, NAA60, NAXE, NFASC, NGLY1, NHLRC1, NKX2-1, NKX6-2, NPC1, NPC2, NPHP1, NPHP3, NPTX1, OFD1, OGDHL, OPA1, OPA3, OPHN1, PACS2, PAX6, PDYN, PEX16, PEX2, PEX6, PGAP2, PGAP3, PGM1, PGM3, PHGDH, PI4KA, PIBF1, PIGA, PIGL, PIGM, PIGN, PIGO, PIGS, PIGT, PIGV, PIGW, PITRM1, PLA2G6, PMM2, PMPCA, PMPCB, PNKD, PNKP, PNPLA6, PNPT1, POC1B, POLG, POLR3A, POLR3B, POLR3K, POMGNT1, POMGNT2, POMK, POMT1, POMT2, POU4F1, PRDM13, PRDX3, PRKCG, PRNP, PRPS1, PRRT2, PTF1A, PTRH2, PUM1, RARS2, RELN, RFT1, RFXANK, RNF170, RNF216, RNF220, ROBO3, RORA, RPGRIP1L, SACS, SAMD9L, SAR1B, SCLT1, SCN1A, SCN2A, SCN8A, SCYL1, SEC23B, SEPSECS, SETX, SIL1, SLC17A5, SLC1A3, SLC25A46, SLC2A1, SLC35A1, SLC35A2, SLC35C1, SLC35D1, SLC37A4, SLC39A8, SLC44A1, SLC52A2, SLC9A1, SLC9A6, SMPD4, SNAP25, SNX14, SPG7, SPR, SPTAN1, SPTBN2, SQSTM1, SRD5A3, SSR3, SSR4, ST3GAL3, ST3GAL5, STT3A, STUB1, SUFU, SVBP, SYNE1, SYNGAP1, TANGO2, TBC1D23, TCTN1, TCTN2, TCTN3, TDP1, TDP2, TECPR2, TERT, TGM6, THG1L, TINF2, TMEM106B, TMEM107, TMEM138, TMEM165, TMEM199, TMEM216, TMEM218, TMEM231, TMEM237, TMEM240, TMEM5, TMEM67, TOE1, TOGARAM1, TPP1, TRAPPC11, TSEN15, TSEN2, TSEN34, TSEN54, TTBK2, TTC19, TTPA, TUBA1A, TUBA4A, TUBA8, TUBB2B, TUBB3, TUBB4A, TUSC3, TWNK, TXNDC15, UBA5, UBTF, UCHL1, VAMP1, VLDLR, VPS13B, VPS13D, VPS41, VPS53, VRK1, WDR73, WDR81, WFS1, WWOX, XRCC1, XYLT1, XYLT2, ZFHX3, ZFYVE26, ZNF423, ZSWIM6					</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>Atrofia muscular espinhal: genes SMN1 e SMN2</title>
		<link>https://genomed.pt/atrofia-muscular-espinhal-genes-smn1-e-smn2/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:13:46 +0000</pubDate>
				<category><![CDATA[Neurologia]]></category>
		<category><![CDATA[Outras metodologias]]></category>
		<category><![CDATA[PTDGF298]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21548</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Atrofia muscular espinhal: genes SMN1 e SMN2" data-especialidade-1="Neurologia" data-especialidade-2="" data-metodologia="MLPA" data-codigo-sns="34900" data-omim="-" data-num-genes="2" data-lista-genes="SMN1, SMN2" data-tat="8 a 10 semanas" 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>

		</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>						MLPA					</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>						SMN1, SMN2					</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>						8 a 10 semanas					</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>Atrofia muscular espinhal: painel de genes por NGS</title>
		<link>https://genomed.pt/atrofia-muscular-espinhal-painel-de-genes-por-ngs/</link>
		
		<dc:creator><![CDATA[Mario Fonte]]></dc:creator>
		<pubDate>Wed, 12 Aug 2020 04:13:55 +0000</pubDate>
				<category><![CDATA[Neurologia]]></category>
		<category><![CDATA[NGS]]></category>
		<category><![CDATA[PTDGF299]]></category>
		<guid isPermaLink="false">https://genomed.pt/?p=21552</guid>

					<description><![CDATA[]]></description>
										<content:encoded><![CDATA[<p><input type="hidden" data-nome-teste="Atrofia muscular espinhal: painel de genes por NGS" data-especialidade-1="Neurologia" data-especialidade-2="" data-metodologia="NGS, com CNVs" data-codigo-sns="34900" data-omim="-" data-num-genes="31" data-lista-genes="AR, ASAH1, ASCC1, ATP7A, BICD2, BSCL2, CHCHD10, DCTN1, DNAJB2, DYNC1H1, EXOSC8, FBXO38, GARS, HSPB1, HSPB8, HSPB3, IGHMBP2, PLEKHG5, RAX2, REEP1, SETX, SIGMAR1, SLC5A7, SMN1, TBCE, TRIP4, TRPV4, UBA1, VAPB, VRK1, WARS" 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>

		</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>						31					</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>						AR, ASAH1, ASCC1, ATP7A, BICD2, BSCL2, CHCHD10, DCTN1, DNAJB2, DYNC1H1, EXOSC8, FBXO38, GARS, HSPB1, HSPB8, HSPB3, IGHMBP2, PLEKHG5, RAX2, REEP1, SETX, SIGMAR1, SLC5A7, SMN1, TBCE, TRIP4, TRPV4, UBA1, VAPB, VRK1, WARS					</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>

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