{"id":9814,"date":"2017-04-29T14:20:16","date_gmt":"2017-04-29T14:20:16","guid":{"rendered":"http:\/\/www.fetaldna.it\/pourquoi-choisir-fetaldna\/"},"modified":"2022-03-10T17:55:57","modified_gmt":"2022-03-10T17:55:57","slug":"porquoi-choisir-fetaldna","status":"publish","type":"page","link":"https:\/\/www.fetaldna.it\/fr\/porquoi-choisir-fetaldna\/","title":{"rendered":"POURQUOI CHOISIR FETALDNA"},"content":{"rendered":"

[vc_row full_width=”stretch_row” content_placement=”middle” softing_bg_attachment=”fixed” softing_lg_bgpos=”center” css=”.vc_custom_1642093982777{padding-top: 100px !important;padding-bottom: 100px !important;background-image: url(https:\/\/www.fetaldna.it\/wp-content\/uploads\/2022\/01\/Sfondo_Altamedica_3.png?id=13453) !important;background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”][vc_column css=”.vc_custom_1641833338705{padding-top: 54px !important;padding-bottom: 100px !important;}”][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_custom_heading text=”TECHNOLOGIE DE POINTE POUR L’ANALYSE DE L’ADN F\u0152TAL” use_theme_fonts=”yes”][vc_column_text]La technologie utilis\u00e9e pour le FetalDNA est reconnue par la communaut\u00e9 scientifique comme la plus avanc\u00e9e au monde<\/strong>, d\u00e9passant les limites des tests d\u00e9j\u00e0 sur le march\u00e9.[\/vc_column_text][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_separator color=”custom” accent_color=”#f2483e”][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_custom_heading text=”D\u00c9COUVREZ LA TECHNOLOGIE NIPT” use_theme_fonts=”yes” link=”url:https%3A%2F%2Fwww.fetaldna.it%2Fnipt-metodologia-inipt%2F|target:_blank”][vc_column_text]L’\u00e9quipe d’Altamedica r\u00e9alise le test pr\u00e9natal gr\u00e2ce \u00e0 des proc\u00e9dures de laboratoire sp\u00e9cifiques:<\/p>\n

R\u00e9ception des pr\u00e9l\u00e8vements de sang<\/p>\n

Isolement de l’ADN f\u0153tal circulant librement du composant maternel<\/p>\n

Analyse multiple de l’ADN par s\u00e9quen\u00e7age massif de derni\u00e8re g\u00e9n\u00e9ration, combinant les plateformes NGS (Next Generation Sequencing) et Digital PCR (Polymerase Chain Reaction)<\/p>\n

Analyse bioinformatique (version 2021<\/em>)<\/p>\n

R\u00e9sultat analytique[\/vc_column_text][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_separator color=”custom” accent_color=”#f2483e”][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_custom_heading text=”UN TEST IMPORTANT POUR UNE GROSSESSE SEREINE” use_theme_fonts=”yes”][vc_row_inner][vc_column_inner width=”1\/4″][vc_column_text]FetalDNA est un test non invasif qui ne pr\u00e9sente absolument aucun risque pour la m\u00e8re ni le f\u0153tus<\/strong>.<\/p>\n

C’est actuellement le test de d\u00e9pistage le plus complet pour l’\u00e9tude des aneuplo\u00efdies chromosomiques affectant le f\u0153tus.
\nPendant la grossesse, certains fragments d’ADN f\u0153tal circulent dans le sang maternel avec une concentration qui augmente sur 9 mois, puis diminue apr\u00e8s l’accouchement. Un niveau optimal pour proc\u00e9der \u00e0 l’ex\u00e9cution de FetalDNA est d\u00e9j\u00e0 obtenu apr\u00e8s 10 semaines<\/strong> de gestation. A ce jour, \u00e0 partir de nos \u00e9tudes de validation clinique, il est possible d’obtenir une tr\u00e8s grande sp\u00e9cificit\u00e9 et sensibilit\u00e9 de l’examen.<\/p>\n

D\u00e8s la 10\u00e8me semaine, il est donc possible de subir un simple pr\u00e9l\u00e8vement sanguin maternel<\/strong>, pour rechercher la pr\u00e9sence d’\u00e9ventuelles anomalies g\u00e9n\u00e9tiques.[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”3\/4″][vc_single_image image=”9823″ img_size=”full”][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_separator color=”custom” accent_color=”#f2483e”][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_custom_heading text=”DES R\u00c9SULTATS RAPIDES, CLAIRES ET FIABLES” use_theme_fonts=”yes”][vc_column_text]Gr\u00e2ce \u00e0 notre technologie de pointe, nous sommes en mesure de garantir des d\u00e9lais de r\u00e9ponse sous 5 jours ouvr\u00e9s<\/strong> pour tous types d’examens (8 jours ouvr\u00e9s dans le cas du FetalDNA \u00c9cran Total).<\/p>\n

Dans les \u00e9tudes de validation pr\u00e9clinique, l’examen a montr\u00e9 une fiabilit\u00e9 de 99,9 % dans la d\u00e9tection de la trisomie 21, de la trisomie 18 et de la trisomie 13, et de 95 % dans la d\u00e9tection de la monosomie X, avec des taux de faux positifs < 0,1 %.<\/p>\n

En particulier, FetalDNA Karyotype<\/a> montre plus de 99% des aneuplo\u00efdies chromosomiques f\u0153tales trouv\u00e9es \u00e0 la naissance, atteignant un niveau de taux de d\u00e9tection comparable \u00e0 l’amniocent\u00e8se et au CVS.<\/p>\n

FetalDNA Karyotype Plus<\/a> est encore plus complet car il ajoute \u00e0 l’\u00e9tude du caryotype un nombre tr\u00e8s \u00e9lev\u00e9 de petits remaniements chromosomiques et le diagnostic de Fibrose kystique Maternelle.<\/p>\n

Les niveaux maximum de sensibilit\u00e9 sont obtenus avec le FetalDNA \u00c9cran Total<\/a>, qui atteint 100% pour la Thrombophilie Maternelle H\u00e9r\u00e9ditaire et pour les infections CMV\/TOXO, 99,9% pour les trisomies des chromosomes 21, 18, 13 et les chromosomes sexuels, 99% pour les maladies monog\u00e9niques, amyotrophie spinale maternelle (SMA) et risque d’accouchement pr\u00e9matur\u00e9.[\/vc_column_text][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/2″][vc_custom_heading text=”<\/p>\n

R\u00c9SULTAT N\u00c9GATIF<\/strong><\/h3>\n

Anomalie g\u00e9n\u00e9tique non d\u00e9tect\u00e9e<\/h4>\n

” font_container=”tag:h3|text_align:left|color:%23f2483e” use_theme_fonts=”yes”][vc_column_text]Le test n’a pas d\u00e9tect\u00e9 d’aneuplo\u00efdie parmi les chromosomes examin\u00e9s ni de microd\u00e9l\u00e9tions. La fiabilit\u00e9 du r\u00e9sultat est rapport\u00e9e dans la section “R\u00e9sultats” du rapport et dans la section “Pr\u00e9cision du test” du rapport technique.[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”1\/2″][vc_custom_heading text=”<\/p>\n

R\u00c9SULTAT POSITIF<\/strong><\/h3>\n

Anomalie g\u00e9n\u00e9tique d\u00e9tect\u00e9e<\/h4>\n

” font_container=”tag:h3|text_align:left|color:%23f2483e” use_theme_fonts=”yes”][vc_column_text]Le test a donn\u00e9 un r\u00e9sultat compatible avec une aneuplo\u00efdie chromosomique f\u0153tale ou avec une microd\u00e9l\u00e9tion. Ce r\u00e9sultat indique que le f\u0153tus pr\u00e9sente l’une des conditions pathologiques indiqu\u00e9es mais, tel qu’\u00e9tabli par les r\u00e8gles minist\u00e9rielles, il doit ensuite \u00eatre confirm\u00e9 par un test de diagnostic invasif.<\/p>\n

Le suivi recommand\u00e9 est un test de diagnostic pr\u00e9natal invasif – amniocent\u00e8se<\/a> ou CVS<\/a> – qui sera r\u00e9alis\u00e9 gratuitement (pr\u00e9l\u00e8vement et analyse) par l\u2019Altamedica Healthcare Center.<\/p>\n

Gr\u00e2ce \u00e0 une consultation g\u00e9n\u00e9tique d\u00e9di\u00e9e, le patient recevra une explication d\u00e9taill\u00e9e des r\u00e9sultats de l’examen. Ce n’est qu’apr\u00e8s confirmation du r\u00e9sultat par amniocent\u00e8se ou CVS qu’il est possible de recourir \u00e0 la loi italienne 194\/78 pour l’interruption volontaire de grossesse.[\/vc_column_text][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"

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