{"id":9684,"date":"2017-08-02T17:12:31","date_gmt":"2017-08-02T17:12:31","guid":{"rendered":"http:\/\/www.fetaldna.it\/fetaldna-cariotipo\/"},"modified":"2024-12-16T15:33:53","modified_gmt":"2024-12-16T15:33:53","slug":"fetaldna-caryotype","status":"publish","type":"page","link":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype\/","title":{"rendered":"FetalDNA CARYOTYPE"},"content":{"rendered":"

[vc_row full_width=”stretch_row” content_placement=”middle” css=”.vc_custom_1641819764103{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_1641819853109{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” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

Le niveau FetalDNA Karyotype \u00e9tudie les aneuplo\u00efdies chromosomiques f\u0153tales de l’ensemble du caryotype.<\/h3>\n

[\/vc_column_text][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/6″][\/vc_column_inner][vc_column_inner width=”2\/3″][vc_custom_heading text=”Alt\u00e9rations dans les 23 paires de chromosomes” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647453333436{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-bottom: 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\/6″][\/vc_column_inner][\/vc_row_inner][vc_separator color=”custom” border_width=”2″ accent_color=”#f2483e”][\/vc_column][\/vc_row][vc_row 0=”” softing_row_prepad=”ptb-30″][vc_column 0=””][vc_column_text]Avec FetalDNA Karyotype<\/strong>, qui dans d’autres tests commerciaux est appel\u00e9 “Kario<\/strong>” ou “eKario<\/strong>” ou “Cario<\/strong>“, est-il possible de rechercher l’existence d’un nombre alt\u00e9r\u00e9 des 46 chromosomes.<\/p>\n

Le niveau FetalDNA Karyotype int\u00e8gre donc l’investigation des aneuplo\u00efdies chromosomiques f\u0153tales li\u00e9es aux autosomes 21, 18, 13 (FetalDNA Base<\/a>)) et aux chromosomes sexuels X, Y (FetalDNA Base Plus<\/a>) avec l’\u00e9valuation bioinformatique de tous les autres chromosomes (tels que appara\u00eet dans l’\u00e9tude classique du caryotype f\u0153tal).<\/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” 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” link=”url:tel%3A068505800|target:_blank”][\/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\/04_TableauComparatif_FetalDNA_Caryotype_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_1641819764103{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_1641819853109{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” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text] Le niveau FetalDNA Karyotype \u00e9tudie les aneuplo\u00efdies chromosomiques f\u0153tales de l’ensemble du caryotype. [\/vc_column_text][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/6″][\/vc_column_inner][vc_column_inner width=”2\/3″][vc_custom_heading text=”Alt\u00e9rations dans les 23 paires de chromosomes” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647453333436{border-top-width:…<\/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-9684","page","type-page","status-publish","hentry"," c-blog-1-item nt-post-class"],"yoast_head":"\nFetalDNA CARYOTYPE - FetalDNA - Altamedica Roma<\/title>\n<meta name=\"description\" content=\"FetalDNA Cariotipo indaga non solo le aneuploidie cromosomiche fetali (21, 18,13, X, Y) ma esamina anche tutte le 23 coppie di cromosomi.\" \/>\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\/\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"FetalDNA CARYOTYPE - FetalDNA - Altamedica Roma\" \/>\n<meta property=\"og:description\" content=\"FetalDNA Cariotipo indaga non solo le aneuploidie cromosomiche fetali (21, 18,13, X, Y) ma esamina anche tutte le 23 coppie di cromosomi.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype\/\" \/>\n<meta property=\"og:site_name\" content=\"FetalDNA\" \/>\n<meta property=\"article:modified_time\" content=\"2024-12-16T15:33:53+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=\"2 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\\\/\",\"url\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/fetaldna-caryotype\\\/\",\"name\":\"FetalDNA CARYOTYPE - FetalDNA - Altamedica Roma\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/#website\"},\"datePublished\":\"2017-08-02T17:12:31+00:00\",\"dateModified\":\"2024-12-16T15:33:53+00:00\",\"description\":\"FetalDNA Cariotipo indaga non solo le aneuploidie cromosomiche fetali (21, 18,13, X, Y) ma esamina anche tutte le 23 coppie di cromosomi.\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/fetaldna-caryotype\\\/#breadcrumb\"},\"inLanguage\":\"fr-FR\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/fetaldna-caryotype\\\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/fetaldna-caryotype\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"FetalDNA CARYOTYPE\"}]},{\"@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":"FetalDNA CARYOTYPE - FetalDNA - Altamedica Roma","description":"FetalDNA Cariotipo indaga non solo le aneuploidie cromosomiche fetali (21, 18,13, X, Y) ma esamina anche tutte le 23 coppie di cromosomi.","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\/","og_locale":"fr_FR","og_type":"article","og_title":"FetalDNA CARYOTYPE - FetalDNA - Altamedica Roma","og_description":"FetalDNA Cariotipo indaga non solo le aneuploidie cromosomiche fetali (21, 18,13, X, Y) ma esamina anche tutte le 23 coppie di cromosomi.","og_url":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype\/","og_site_name":"FetalDNA","article_modified_time":"2024-12-16T15:33:53+00:00","twitter_card":"summary_large_image","twitter_misc":{"Dur\u00e9e de lecture estim\u00e9e":"2 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype\/","url":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype\/","name":"FetalDNA CARYOTYPE - FetalDNA - Altamedica Roma","isPartOf":{"@id":"https:\/\/www.fetaldna.it\/#website"},"datePublished":"2017-08-02T17:12:31+00:00","dateModified":"2024-12-16T15:33:53+00:00","description":"FetalDNA Cariotipo indaga non solo le aneuploidie cromosomiche fetali (21, 18,13, X, Y) ma esamina anche tutte le 23 coppie di cromosomi.","breadcrumb":{"@id":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype\/#breadcrumb"},"inLanguage":"fr-FR","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.fetaldna.it\/fr\/fetaldna-caryotype\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.fetaldna.it\/fr\/"},{"@type":"ListItem","position":2,"name":"FetalDNA CARYOTYPE"}]},{"@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\/9684","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=9684"}],"version-history":[{"count":9,"href":"https:\/\/www.fetaldna.it\/fr\/wp-json\/wp\/v2\/pages\/9684\/revisions"}],"predecessor-version":[{"id":15250,"href":"https:\/\/www.fetaldna.it\/fr\/wp-json\/wp\/v2\/pages\/9684\/revisions\/15250"}],"wp:attachment":[{"href":"https:\/\/www.fetaldna.it\/fr\/wp-json\/wp\/v2\/media?parent=9684"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}