{"id":9904,"date":"2017-08-02T17:34:50","date_gmt":"2017-08-02T17:34:50","guid":{"rendered":"http:\/\/www.fetaldna.it\/fetaldna-cariotipo-plus\/"},"modified":"2024-12-16T15:38:02","modified_gmt":"2024-12-16T15:38:02","slug":"fetaldna-caryotype-plus","status":"publish","type":"page","link":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype-plus\/","title":{"rendered":"FetalDNA Caryotype Plus"},"content":{"rendered":"

[vc_row full_width=”stretch_row” content_placement=”middle” css=”.vc_custom_1641823847050{padding-top: 100px !important;padding-bottom: 50px !important;background-image: url(https:\/\/www.fetaldna.it\/wp-content\/uploads\/2019\/04\/header_mom.jpg?id=10022) !important;background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”][vc_column css=”.vc_custom_1641823491029{padding-top: 100px !important;padding-bottom: 100px !important;}”][\/vc_column][\/vc_row][vc_row 0=”” softing_row_prepad=”ptb-30″][vc_column 0=””][vc_custom_heading text=”FETALDNA CARYOTYPE PLUS” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

Le niveau FetalDNA Karyotype Plus est le test pr\u00e9natal non invasif (NIPT) le plus \u00e9lev\u00e9 disponible aujourd’hui sur l’ADN f\u0153tal, \u00e0 l’exception du FetalDNA Total Screen.<\/h3>\n

[\/vc_column_text][\/vc_column][\/vc_row][vc_row 0=””][vc_column 0=”” width=”1\/3″][vc_custom_heading text=”Caryotype
\nf\u0153tal” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647453807159{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column][vc_column width=”1\/3″][vc_custom_heading text=”syndromes de
\nmicrod\u00e9l\u00e9tion \/ microduplication” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647453834783{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column][vc_column width=”1\/3″][vc_custom_heading text=”Fibrose kystique
\nmaternelle” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647453850188{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column][\/vc_row][vc_row 0=””][vc_column 0=””][vc_separator color=”custom” accent_color=”#f2483e”][\/vc_column][\/vc_row][vc_row 0=”” softing_row_prepad=”ptb-30″][vc_column 0=””][vc_column_text]FetalDNA Karyotype Plus<\/strong> est l’un des niveaux les plus complets en tant que test pr\u00e9natal : il ajoute \u00e0 toutes les investigations pr\u00e9c\u00e9dentes le screening d’un grand nombre d’alt\u00e9rations chromosomiques caus\u00e9es par des r\u00e9arrangements structurels (qui sont d\u00e9finis comme des microduplications \/ microd\u00e9l\u00e9tions) \u00e0 une r\u00e9solution d’environ 7 Mb (pour les r\u00e9solutions, un diagnostic inf\u00e9rieur sur le sang maternel n’est pas obtenu, seul un diagnostic pr\u00e9natal invasif tel que l’amniocent\u00e8se ou le CVS doit \u00eatre utilis\u00e9, en r\u00e9alisant une \u00e9tude sp\u00e9cifique avec des puces \u00e0 ADN).<\/p>\n

En bref, avec le niveau Karyotype Plus, les alt\u00e9rations num\u00e9riques des 23 paires de chromosomes du f\u0153tus sont analys\u00e9es (y compris les trisomies des chromosomes 13, 18, 21 et les anomalies des chromosomes sexuels X et Y, d\u00e9terminant \u00e9galement le sexe f\u0153tal sur demande) et, gr\u00e2ce \u00e0 une \u00e9valuation bioinformatique particuli\u00e8re, il est \u00e9galement possible d’inspecter la structure interne des chromosomes, avec d\u00e9finition de l’ordre des m\u00e9gabases.<\/p>\n

FetalDNA Karyotype Plus<\/strong> est \u00e9galement en mesure d’\u00e9largir l’investigation des pathologies avec un screening qui permet d’obtenir des informations sur la pr\u00e9sence des syndromes de microd\u00e9l\u00e9tion<\/a><\/strong> les plus importants chez le f\u0153tus.<\/p>\n

Le terme microd\u00e9l\u00e9tion \/ microduplications fait r\u00e9f\u00e9rence \u00e0 des anomalies caract\u00e9ris\u00e9es par l’absence d’un petit tractus chromosomique entra\u00eenant une perte d’informations g\u00e9n\u00e9tiques (microd\u00e9l\u00e9tions) ou par l’ajout de mat\u00e9riel g\u00e9nomique surnum\u00e9raire (microduplications). Les deux conditions provoquent des pathologies avec des images cliniques et ph\u00e9notypiques complexes et variables selon le chromosome impliqu\u00e9, la r\u00e9gion chromosomique impliqu\u00e9e et la taille de la microd\u00e9l\u00e9tion \/ microduplication elle-m\u00eame.<\/p>\n

Les principaux syndromes de microd\u00e9l\u00e9tion \u00e9tudi\u00e9s par le FetalDNA Karyotype Plus sont list\u00e9s ci-dessous:[\/vc_column_text][\/vc_column][\/vc_row][vc_row 0=”” softing_row_prepad=”ptb-30″ el_id=”microdelezione2″][vc_column 0=””][vc_row_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de d\u00e9l\u00e9tion 1q21.1″ font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454000727{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Prader Willi” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454010702{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome du Cri-du-chat” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454026332{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Miller-Dieker” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454048143{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome WAGR” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454064803{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Potocki-Shaffer” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454081614{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome d’Angelman” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454090759{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Rubinstein-Taybi” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454100695{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Koolen de Vries” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454112212{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de d\u00e9l\u00e9tion 18q” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454123197{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome d’Alagille (AGS)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454136810{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de d\u00e9l\u00e9tion 1p36″ font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454148178{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Kleefstra (SK)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454165107{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Phelan-Mcdermid” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454179875{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Smith-Magenis” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454191049{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de d\u00e9l\u00e9tion 1q21.1″ font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454204639{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Di George” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454218552{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Jacobsen” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454230216{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Langer-Giedion” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454239756{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Wolf-Hirschhorn” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454250079{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/4″][vc_custom_heading text=”Neuropathie h\u00e9r\u00e9ditaire avec susceptibilit\u00e9 \u00e0 la paralysie de pression (HNPP)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454260454{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/4″][\/vc_column_inner][vc_column_inner width=”1\/4″][\/vc_column_inner][vc_column_inner width=”1\/4″][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row 0=”” softing_row_prepad=”ptb-30″][vc_column 0=””][vc_column_text]<\/p>\n

Le FetalDNA Karyotype Plus comprend \u00e9galement, gratuitement, la recherche des mutations les plus fr\u00e9quentes de la Fibrose kystique Maternelle.<\/h3>\n

[\/vc_column_text][vc_column_text]Ainsi, si l’une de ces mutations est pr\u00e9sente chez la m\u00e8re, il faudra rechercher si le f\u0153tus est \u00e9galement porteur simple ou, si le p\u00e8re \u00e9tait \u00e9galement porteur, a couru le risque d’\u00eatre atteint de fibrose kystique. Cela se produit dans 25 % des cas si les deux parents \u00e9taient porteurs sains.<\/p>\n

Avec le FetalDNA Karyotype Plus<\/strong>, l’analyse du g\u00e8ne maternel est r\u00e9alis\u00e9e \u00e0 travers un d\u00e9pistage appel\u00e9 1er niveau qui permet d’analyser les mutations les plus courantes et les plus fr\u00e9quentes, parvenant \u00e0 identifier environ 83% des porteurs. La fr\u00e9quence estim\u00e9e, dans la population italienne, des porteurs sains (souvent inconscients de l’\u00eatre) est de 1 sur 25-30, celle des naissances atteintes est de 1 sur 2500 – 3000.<\/p>\n

Sexe de l’enfant disponible sur demande.<\/em>[\/vc_column_text][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column width=”1\/4″][\/vc_column][vc_column width=”1\/2″][vc_btn title=”DEMANDEZ UNE CONSULTATION” style=”effect” link=”url:tel%3A068505800|target:_blank” softing_vc_btn_brdclr=”#f2483e” softing_vc_btn_hvrbrdclr=”#f2483e” softing_vc_btn_bg=”#f2483e” softing_vc_btn_hvrbg=”#ffffff” softing_vc_btn_title=”#ffffff” softing_vc_btn_hvrtitle=”#f2483e”][\/vc_column][vc_column width=”1\/4″][\/vc_column][\/vc_row][vc_row][vc_column][vc_message message_box_color=”grey”]<\/p>\n

Les r\u00e9sultats sont disponibles sous 5 jours ouvr\u00e9s (mais le d\u00e9lai peut s’allonger en cas de difficult\u00e9s techniques lors de l’analyse ADN ou si le patient doit refaire le test).<\/h4>\n

Le test pr\u00e9natal r\u00e9alise un d\u00e9pistage sophistiqu\u00e9 et fiable mais pas un diagnostic, quelles que soient l’entreprise et la technologie utilis\u00e9es. La certitude diagnostique n’est fournie que par des tests invasifs (amniocent\u00e8se et CVS) comme indiqu\u00e9 dans toutes les lignes directrices et la litt\u00e9rature scientifique internationale.<\/h4>\n

Dans le cas o\u00f9 le test de d\u00e9pistage ADN (Base FetalDNA) r\u00e9v\u00e8le des anomalies, l\u2019Altamedica Healthcare Center propose des tests de confirmation gratuits par diagnostic pr\u00e9natal (CVS ou Amniocent\u00e8se).<\/h4>\n

[\/vc_message][\/vc_column][\/vc_row][vc_row full_width=”stretch_row_content” softing_row_prepad=”ptb-30″][vc_column][vc_custom_heading text=”TABLEAU COMPARATIF” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_single_image source=”external_link” alignment=”center” custom_src=”https:\/\/www.fetaldna.it\/img\/05_TableauComparatif_FetalDNA_Caryotype_Plus_FR.png”][\/vc_column][\/vc_row][vc_row 0=”” softing_row_prepad=”ptb-30″ el_id=”monogeniche”][vc_column 0=””][vc_separator color=”custom” accent_color=”#f2483e”][\/vc_column][\/vc_row][vc_row 0=”” softing_row_prepad=”ptb-30″][vc_column 0=””][vc_custom_heading text=”FetalDNA Caryotype Plus + Maladies f\u0153tales monog\u00e9niques” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

Il est \u00e9galement possible d’int\u00e9grer \u00e0 ce niveau le d\u00e9pistage des Maladies F\u0153tales Monog\u00e9niques:<\/h4>\n

[\/vc_column_text][\/vc_column][\/vc_row][vc_row 0=”” softing_row_prepad=”ptb-30″][vc_column 0=””][vc_row_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Fibrose kystique (GENE CFTR)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454426017{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Surdit\u00e9 cong\u00e9nitale (GENE GJB2)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454440406{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”B\u00eata-thalass\u00e9mie (GENE HBB)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454450978{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Syndrome de Rett (GENE MECP2)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454460551{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”H\u00e9mochromatose (GENE HFE)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454472869{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Achondroplasie (GENE FGFR3)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454482861{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Hypochondroplasie (GENE FGFR3)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454492659{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Dysplasie thanatophorique (GENE FGFR3)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454503714{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Syndrome d’Apert (GENE FGFR2)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454519246{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Syndrome de Crouzon (GENE FGFR2)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454536230{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Syndrome du l\u00e9opard (g\u00e8ne PTPN11)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454547656{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Ph\u00e9nylc\u00e9tonurie (G\u00c8NE PAH)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454562146{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Syndrome de Noonan
\n(GENES PTPN11 \/ SOS1 \/ RAF1)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454580722{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Hyperplasie cong\u00e9nitale classique des surr\u00e9nales par d\u00e9ficit en 21-hydroxylase (GENE CYP21A2)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454594556{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Rein polykystique autosomique r\u00e9cessif (PKHD1)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647454612353{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-width: 2px !important;padding-top: 5% !important;padding-right: 5% !important;padding-bottom: 5% !important;padding-left: 5% !important;background-color: #f7f7f7 !important;border-left-color: #f0f0f0 !important;border-left-style: solid !important;border-right-color: #f0f0f0 !important;border-right-style: solid !important;border-top-color: #f0f0f0 !important;border-top-style: solid !important;border-bottom-color: #f0f0f0 !important;border-bottom-style: solid !important;border-radius: 5px !important;}”][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column width=”1\/4″][\/vc_column][vc_column width=”1\/2″][vc_btn title=”DEMANDEZ UNE CONSULTATION” style=”effect” link=”url:tel%3A068505800|target:_blank” softing_vc_btn_brdclr=”#f2483e” softing_vc_btn_hvrbrdclr=”#f2483e” softing_vc_btn_bg=”#f2483e” softing_vc_btn_hvrbg=”#ffffff” softing_vc_btn_title=”#ffffff” softing_vc_btn_hvrtitle=”#f2483e”][\/vc_column][vc_column width=”1\/4″][\/vc_column][\/vc_row][vc_row][vc_column][vc_message message_box_color=”grey”]<\/p>\n

Les r\u00e9sultats sont disponibles sous 5 jours ouvr\u00e9s (mais le d\u00e9lai peut s’allonger en cas de difficult\u00e9s techniques lors de l’analyse ADN ou si le patient doit refaire le test).<\/h4>\n

Le test pr\u00e9natal r\u00e9alise un d\u00e9pistage sophistiqu\u00e9 et fiable mais pas un diagnostic, quelles que soient l’entreprise et la technologie utilis\u00e9es. La certitude diagnostique n’est fournie que par des tests invasifs (amniocent\u00e8se et CVS) comme indiqu\u00e9 dans toutes les lignes directrices et la litt\u00e9rature scientifique internationale.<\/h4>\n

Dans le cas o\u00f9 le test de d\u00e9pistage ADN (Base FetalDNA) r\u00e9v\u00e8le des anomalies, l\u2019Altamedica Healthcare Center propose des tests de confirmation gratuits par diagnostic pr\u00e9natal (CVS ou Amniocent\u00e8se).<\/h4>\n

[\/vc_message][\/vc_column][\/vc_row][vc_row full_width=”stretch_row_content” softing_row_prepad=”ptb-30″][vc_column][vc_custom_heading text=”TABLEAU COMPARATIF” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_single_image source=”external_link” alignment=”center” custom_src=”https:\/\/www.fetaldna.it\/img\/06_TableauComparatif_FetalDNA_Caryotype_Plus+monogeniques_FR.png”][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"

[vc_row full_width=”stretch_row” content_placement=”middle” css=”.vc_custom_1641823847050{padding-top: 100px !important;padding-bottom: 50px !important;background-image: url(https:\/\/www.fetaldna.it\/wp-content\/uploads\/2019\/04\/header_mom.jpg?id=10022) !important;background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”][vc_column css=”.vc_custom_1641823491029{padding-top: 100px !important;padding-bottom: 100px !important;}”][\/vc_column][\/vc_row][vc_row 0=”” softing_row_prepad=”ptb-30″][vc_column 0=””][vc_custom_heading text=”FETALDNA CARYOTYPE PLUS” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text] Le niveau FetalDNA Karyotype Plus est le test pr\u00e9natal non invasif (NIPT) le plus \u00e9lev\u00e9 disponible aujourd’hui sur l’ADN f\u0153tal, \u00e0 l’exception du FetalDNA Total Screen….<\/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-9904","page","type-page","status-publish","hentry"," c-blog-1-item nt-post-class"],"yoast_head":"\nCariotipo Plus - Test DNA fetale FetalDNA - Altamedica Roma<\/title>\n<meta name=\"description\" content=\"FetalDNA Cariotipo Plus aggiunge ai livelli precendenti di analisi DNA fetale anche lo screening di microduplicazioni \/ microdelezioni.\" \/>\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\/fetaldna-caryotype-plus\/\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Cariotipo Plus - Test DNA fetale FetalDNA - Altamedica Roma\" \/>\n<meta property=\"og:description\" content=\"FetalDNA Cariotipo Plus aggiunge ai livelli precendenti di analisi DNA fetale anche lo screening di microduplicazioni \/ microdelezioni.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype-plus\/\" \/>\n<meta property=\"og:site_name\" content=\"FetalDNA\" \/>\n<meta property=\"article:modified_time\" content=\"2024-12-16T15:38:02+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Dur\u00e9e de lecture estim\u00e9e\" \/>\n\t<meta name=\"twitter:data1\" content=\"14 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/fetaldna-caryotype-plus\\\/\",\"url\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/fetaldna-caryotype-plus\\\/\",\"name\":\"Cariotipo Plus - Test DNA fetale FetalDNA - Altamedica Roma\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/#website\"},\"datePublished\":\"2017-08-02T17:34:50+00:00\",\"dateModified\":\"2024-12-16T15:38:02+00:00\",\"description\":\"FetalDNA Cariotipo Plus aggiunge ai livelli precendenti di analisi DNA fetale anche lo screening di microduplicazioni \\\/ microdelezioni.\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/fetaldna-caryotype-plus\\\/#breadcrumb\"},\"inLanguage\":\"fr-FR\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/fetaldna-caryotype-plus\\\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/fetaldna-caryotype-plus\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"FetalDNA Caryotype Plus\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/#website\",\"url\":\"https:\\\/\\\/www.fetaldna.it\\\/\",\"name\":\"FetalDNA | Il test prenatale su DNA fetale\",\"description\":\"Il test prenatale di ultima generazione\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/www.fetaldna.it\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"fr-FR\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Cariotipo Plus - Test DNA fetale FetalDNA - Altamedica Roma","description":"FetalDNA Cariotipo Plus aggiunge ai livelli precendenti di analisi DNA fetale anche lo screening di microduplicazioni \/ microdelezioni.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype-plus\/","og_locale":"fr_FR","og_type":"article","og_title":"Cariotipo Plus - Test DNA fetale FetalDNA - Altamedica Roma","og_description":"FetalDNA Cariotipo Plus aggiunge ai livelli precendenti di analisi DNA fetale anche lo screening di microduplicazioni \/ microdelezioni.","og_url":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype-plus\/","og_site_name":"FetalDNA","article_modified_time":"2024-12-16T15:38:02+00:00","twitter_card":"summary_large_image","twitter_misc":{"Dur\u00e9e de lecture estim\u00e9e":"14 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype-plus\/","url":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype-plus\/","name":"Cariotipo Plus - Test DNA fetale FetalDNA - Altamedica Roma","isPartOf":{"@id":"https:\/\/www.fetaldna.it\/#website"},"datePublished":"2017-08-02T17:34:50+00:00","dateModified":"2024-12-16T15:38:02+00:00","description":"FetalDNA Cariotipo Plus aggiunge ai livelli precendenti di analisi DNA fetale anche lo screening di microduplicazioni \/ microdelezioni.","breadcrumb":{"@id":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype-plus\/#breadcrumb"},"inLanguage":"fr-FR","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype-plus\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype-plus\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.fetaldna.it\/fr\/"},{"@type":"ListItem","position":2,"name":"FetalDNA Caryotype Plus"}]},{"@type":"WebSite","@id":"https:\/\/www.fetaldna.it\/#website","url":"https:\/\/www.fetaldna.it\/","name":"FetalDNA | Il test prenatale su DNA fetale","description":"Il test prenatale di ultima generazione","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.fetaldna.it\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"fr-FR"}]}},"_links":{"self":[{"href":"https:\/\/www.fetaldna.it\/fr\/wp-json\/wp\/v2\/pages\/9904","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.fetaldna.it\/fr\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.fetaldna.it\/fr\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.fetaldna.it\/fr\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.fetaldna.it\/fr\/wp-json\/wp\/v2\/comments?post=9904"}],"version-history":[{"count":15,"href":"https:\/\/www.fetaldna.it\/fr\/wp-json\/wp\/v2\/pages\/9904\/revisions"}],"predecessor-version":[{"id":15255,"href":"https:\/\/www.fetaldna.it\/fr\/wp-json\/wp\/v2\/pages\/9904\/revisions\/15255"}],"wp:attachment":[{"href":"https:\/\/www.fetaldna.it\/fr\/wp-json\/wp\/v2\/media?parent=9904"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}