{"id":9664,"date":"2017-04-28T21:48:45","date_gmt":"2017-04-28T21:48:45","guid":{"rendered":"http:\/\/www.fetaldna.it\/il-test-fetaldna\/"},"modified":"2024-12-16T15:32:39","modified_gmt":"2024-12-16T15:32:39","slug":"test-dna-fetale-fetaldna","status":"publish","type":"page","link":"https:\/\/www.fetaldna.it\/fr\/test-dna-fetale-fetaldna\/","title":{"rendered":"DE QUOI S&#8217;AGIT-IL"},"content":{"rendered":"<div class=\"wpb-content-wrapper\"><p>[vc_row 0=&#8221;&#8221; full_width=&#8221;stretch_row&#8221; equal_height=&#8221;yes&#8221;][vc_column 0=&#8221;&#8221;][vc_custom_heading text=&#8221;DE QUOI S&#8217;AGIT-IL&#8221; font_container=&#8221;tag:h2|text_align:center&#8221; use_theme_fonts=&#8221;yes&#8221;][vc_row_inner][vc_column_inner width=&#8221;1\/2&#8243;][vc_column_text]<strong>FetalDNA<\/strong> est un test de screening pr\u00e9natal non invasif (NIPT) bas\u00e9 sur l&#8217;analyse de l&#8217;ADN f\u0153tal libre circulant sur le sang maternel, afin de d\u00e9tecter les aneuplo\u00efdies f\u0153tales les plus fr\u00e9quentes pendant la grossesse telles que celles li\u00e9es au chromosome 21 (syndrome de Down), au chromosome 18 (syndrome d&#8217;Edwards), le chromosome 13 (syndrome de Patau) et les chromosomes sexuels X et Y (syndrome de Turner, Klinefelter).<\/p>\n<p><strong>Le test d&#8217;ADN f\u0153tal FetalDNA<\/strong> fournit <strong>8 niveaux d&#8217;investigation de l&#8217;ADN f\u0153tal<\/strong>, avec un degr\u00e9 croissant de profondeur.<\/p>\n<p>Du premier &#8211; <a href=\"https:\/\/www.fetaldna.it\/fr\/fetaldna-base\/\" target=\"_blank\" rel=\"noopener\"><strong>FetalDNA Base<\/strong><\/a> &#8211; qui \u00e9tudie les anomalies chromosomiques les plus fr\u00e9quentes telles que le syndrome de Down, le syndrome d&#8217;Edwards et le syndrome de Patau, jusqu&#8217;au plus avanc\u00e9 &#8211; <a href=\"https:\/\/www.fetaldnatotalscreen.it\/\" target=\"_blank\" rel=\"noopener\">FetalDNA Total Screen<\/a> &#8211; qui permet le d\u00e9pistage g\u00e9n\u00e9tique le plus complet pendant la grossesse, en plus des informations sur l&#8217;ensemble chromosomique du f\u0153tus et les alt\u00e9rations structurelles associ\u00e9es \u00e0 diverses conditions pathologiques.[\/vc_column_text][vc_column_text]<\/p>\n<div class=\"wpb_text_column wpb_content_element \">\n<div class=\"wpb_wrapper\">\n<p><em>Sur demande, il est possible d&#8217;obtenir le facteur HR de l&#8217;enfant.<\/em><\/p>\n<\/div>\n<\/div>\n<p>[\/vc_column_text][\/vc_column_inner][vc_column_inner width=&#8221;1\/2&#8243;][vc_video link=&#8221;https:\/\/youtu.be\/bi7cXAetSvo&#8221; align=&#8221;center&#8221;][vc_column_text css=&#8221;.vc_custom_1646602172065{padding-top: 5% !important;}&#8221;]En particulier, <a href=\"https:\/\/www.fetaldna.it\/fr\/fetaldna-base\/\" target=\"_blank\" rel=\"noopener\"><strong>FetalDNA Base<\/strong><\/a>\u00a0 s&#8217;adresse \u00e9galement \u00e0 ceux qui effectuent la clart\u00e9 nucale lors du screening du premier trimestre de la grossesse, d\u00e9passant d\u00e9finitivement les limites importantes des tests combin\u00e9s (\u00e9chographie et biochimique). Ce test a un co\u00fbt tr\u00e8s accessible et apporte une r\u00e9ponse extr\u00eamement rapide.[\/vc_column_text][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row 0=&#8221;&#8221; full_width=&#8221;stretch_row_content&#8221; softing_row_prepad=&#8221;ptb-30&#8243;][vc_column 0=&#8221;&#8221;][vc_separator color=&#8221;custom&#8221; border_width=&#8221;2&#8243; accent_color=&#8221;#f2483e&#8221;][vc_custom_heading text=&#8221;TABLEAU COMPARATIF&#8221; font_container=&#8221;tag:h2|text_align:center&#8221; use_theme_fonts=&#8221;yes&#8221; css=&#8221;.vc_custom_1646602469059{padding-top: 3% !important;}&#8221;][vc_single_image source=&#8221;external_link&#8221; alignment=&#8221;center&#8221; custom_src=&#8221;https:\/\/www.fetaldna.it\/img\/00_TableauComparatif_FetalDNA_FR.png&#8221;][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row 0=&#8221;&#8221; full_width=&#8221;stretch_row&#8221; equal_height=&#8221;yes&#8221;][vc_column 0=&#8221;&#8221;][vc_custom_heading text=&#8221;DE QUOI S&#8217;AGIT-IL&#8221; font_container=&#8221;tag:h2|text_align:center&#8221; use_theme_fonts=&#8221;yes&#8221;][vc_row_inner][vc_column_inner width=&#8221;1\/2&#8243;][vc_column_text]FetalDNA est un test de screening pr\u00e9natal non invasif (NIPT) bas\u00e9 sur l&#8217;analyse de l&#8217;ADN f\u0153tal libre circulant sur le sang maternel, afin de d\u00e9tecter les aneuplo\u00efdies f\u0153tales les plus fr\u00e9quentes pendant la grossesse telles que celles li\u00e9es au chromosome 21 (syndrome de Down), au&#8230;<\/p>\n","protected":false},"author":3,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"custom-page.php","meta":{"footnotes":""},"class_list":["post-9664","page","type-page","status-publish","hentry"," c-blog-1-item  nt-post-class"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Test del DNA fetale - FetalDNA: che cos&#039;\u00e8 - Altamedica Roma<\/title>\n<meta name=\"description\" content=\"Che cos&#039;\u00e8 il test del DNA fetale FetalDNA e quali sono le anomalie genetiche fetali che individua. Prenota il tuo screening: 06 8505800.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.fetaldna.it\/fr\/test-dna-fetale-fetaldna\/\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Test del DNA fetale - FetalDNA: che cos&#039;\u00e8 - Altamedica Roma\" \/>\n<meta property=\"og:description\" content=\"Che cos&#039;\u00e8 il test del DNA fetale FetalDNA e quali sono le anomalie genetiche fetali che individua. 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