{"id":9674,"date":"2018-04-18T16:38:14","date_gmt":"2018-04-18T16:38:14","guid":{"rendered":"http:\/\/www.fetaldna.it\/fetaldna-base-plus-2\/"},"modified":"2024-12-16T15:33:42","modified_gmt":"2024-12-16T15:33:42","slug":"fetaldna-base-plus-2","status":"publish","type":"page","link":"https:\/\/www.fetaldna.it\/fr\/fetaldna-base-plus-2\/","title":{"rendered":"FETALDNA BASE PLUS"},"content":{"rendered":"

[vc_row full_width=”stretch_row” content_placement=”middle” css=”.vc_custom_1641815715741{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_1641815663675{padding-top: 100px !important;padding-bottom: 100px !important;}”][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_custom_heading text=”FetalDNA Base Plus” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

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Le FetalDNA Base Plus \u00e9tudie les 3 principales aneuplo\u00efdies chromosomiques f\u0153tales li\u00e9es aux chromosomes 21, 18,13 et aux chromosomes sexuels X, Y et au sexe f\u0153tal.<\/h3>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n

[\/vc_column_text][\/vc_column][\/vc_row][vc_row content_placement=”middle” softing_row_prepad=”ptb-30″][vc_column width=”1\/4″][vc_custom_heading text=”Syndrome de Down” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647383238444{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_text]<\/p>\n

Trisomie du chromosome 21<\/strong><\/p>\n

C’est l’une des aneuplo\u00efdies les plus courantes; il fait r\u00e9f\u00e9rence \u00e0 la pr\u00e9sence d’une copie suppl\u00e9mentaire du chromosome 21.<\/p>\n

[\/vc_column_text][\/vc_column][vc_column width=”1\/4″][vc_custom_heading text=”Syndrome d’Edwards” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647383278555{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_text]<\/p>\n

Trisomie du chromosome 18<\/strong><\/p>\n

Pr\u00e9sence d’une copie suppl\u00e9mentaire du chromosome 18.<\/p>\n

[\/vc_column_text][\/vc_column][vc_column width=”1\/4″][vc_custom_heading text=”Syndrome de Patau” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647383318448{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_text]<\/p>\n

Trisomie du chromosome 13<\/strong><\/p>\n

Pr\u00e9sence d’une copie suppl\u00e9mentaire du chromosome 13.<\/p>\n

[\/vc_column_text][\/vc_column][vc_column width=”1\/4″][vc_custom_heading text=”Chromosomes X, Y” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647383351345{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_text]<\/p>\n

Aneuplo\u00efdies des chromosomes sexuels<\/strong><\/p>\n

Anomalies num\u00e9riques des chromosomes sexuels.<\/p>\n

[\/vc_column_text][\/vc_column][\/vc_row][vc_row][vc_column][vc_separator color=”custom” border_width=”2″ accent_color=”#f2483e”][vc_column_text css=”.vc_custom_1667585024557{padding-top: 5% !important;}”]<\/p>\n

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Par rapport \u00e0 la FetalDNA Base<\/a>, la FetalDNA Base Plus int\u00e8gre les aneuplodies des chromosomes sexuels<\/em> (anomalies affectant les chromosomes sexuels X, Y) qui peuvent entra\u00eener des difficult\u00e9s de langage, de mouvement et\/ou d’apprentissage chez l’enfant.<\/p>\n

La plus courante de cette classe d’aneuplo\u00efdie est le syndrome de Turner<\/em> ou la monosomie li\u00e9e \u00e0 l’X<\/em> qui affecte les femmes avec une seule copie du chromosome X.<\/p>\n

Les autres aneuplodias trouv\u00e9es avec le FetalDNA Base Plus sont la trisomie du chromosome<\/em> X (XXX), le syndrome de Klinefelter<\/em> et le syndrome de Jacobs<\/em>.<\/p>\n

Sexe de l’enfant disponible sur demande.<\/em><\/p>\n

Aucune information n’est fournie sur les autres anomalies chromosomiques.<\/em><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n

[\/vc_column_text][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/4″][\/vc_column_inner][vc_column_inner width=”1\/2″][vc_btn title=”DEMANDEZ UNE CONSULTATION” style=”effect” size=”lg” softing_vc_btn_brdstyle=”solid” link=”url:tel%3A068505800″ 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_inner][vc_column_inner width=”1\/4″][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][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\/02_TableauComparatif_FetalDNA_BasePlus_FR.png”][\/vc_column][\/vc_row][vc_row content_placement=”top” softing_row_prepad=”ptb-30″ el_id=”microdelezioni2″][vc_column][vc_separator color=”custom” border_width=”2″ accent_color=”#f2483e”][\/vc_column][\/vc_row][vc_row][vc_column][vc_custom_heading text=”BASE PLUS + 90 MICRODELETIONS” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

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Il est \u00e9galement possible de combiner ce niveau avec la recherche de 90 microd\u00e9l\u00e9tions, qui sont des anomalies caract\u00e9ris\u00e9es par l’absence d’un petit tractus chromosomique avec pour cons\u00e9quence une perte d’information g\u00e9nique (microd\u00e9l\u00e9tions) ou par l’ajout de mat\u00e9riel g\u00e9nomique surnum\u00e9raire (microduplications)<\/h4>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n

[\/vc_column_text][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_row_inner equal_height=”yes”][vc_column_inner width=”1\/4″][vc_custom_heading text=”Syndrome de Di George” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1647383807953{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383820207{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383827955{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383836839{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383848368{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383859278{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383870406{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383882719{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383898004{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383907580{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383916826{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383927719{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383941682{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383956816{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383966724{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:left” use_theme_fonts=”yes” css=”.vc_custom_1647383978122{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 Williams” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1647383988789{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
\n(suppression 5p)” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1647384016396{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
\n(15q11-q13)” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1647384026954{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=”Neuropathie h\u00e9r\u00e9ditaire avec susceptibilit\u00e9 \u00e0 la paralysie de pression (HNPP)” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1647384045925{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 Miller-Dieker ou lissenc\u00e9phalie de type 1 \u00e0 partir d’anomalies LIS 1 ou syndrome de Miller-Dieker (MDS)” font_container=”tag:h5|text_align:left” use_theme_fonts=”yes” css=”.vc_custom_1647384059471{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_text]<\/p>\n

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Sexe de l’enfant disponible sur demande.<\/em><\/p>\n

Aucune information n’est fournie sur les autres anomalies chromosomiques.<\/em><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n

[\/vc_column_text][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/4″][\/vc_column_inner][vc_column_inner width=”1\/2″][vc_btn title=”DEMANDEZ UNE CONSULTATION” style=”effect” size=”lg” softing_vc_btn_brdstyle=”solid” link=”url:tel%3A068505800″ 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_inner][vc_column_inner width=”1\/4″][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row][vc_column][vc_message message_box_color=”grey”]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).<\/p>\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.<\/p>\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[\/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\/03_TableauComparatif_FetalDNA_BasePlus90_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_1641815715741{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_1641815663675{padding-top: 100px !important;padding-bottom: 100px !important;}”][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][vc_custom_heading text=”FetalDNA Base Plus” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text] Le FetalDNA Base Plus \u00e9tudie les 3 principales aneuplo\u00efdies chromosomiques f\u0153tales li\u00e9es aux chromosomes 21, 18,13 et aux chromosomes sexuels X, Y et au sexe f\u0153tal. 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