{"id":9767,"date":"2017-08-02T16:40:08","date_gmt":"2017-08-02T16:40:08","guid":{"rendered":"http:\/\/www.fetaldna.it\/fetaldna-base\/"},"modified":"2024-12-16T15:33:06","modified_gmt":"2024-12-16T15:33:06","slug":"nipt-mini-inipt-2","status":"publish","type":"page","link":"https:\/\/www.fetaldna.it\/fr\/nipt-mini-inipt-2\/","title":{"rendered":"FetalDNA Base"},"content":{"rendered":"

[vc_row full_width=”stretch_row” content_placement=”middle” css=”.vc_custom_1641815422294{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_1641815492985{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 Base” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

Le niveau FetalDNA Base \u00e9tudie les anomalies chromosomiques les plus courantes (aneuplo\u00efdies).<\/h3>\n

[\/vc_column_text][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/3″][vc_custom_heading text=”Syndrome de Down” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647382272356{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_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Syndrome d’Edwards” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647382316731{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_inner][vc_column_inner width=”1\/3″][vc_custom_heading text=”Syndrome de Patau” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647382353528{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_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row 0=”” full_width=”stretch_row”][vc_column 0=””][vc_separator color=”custom” border_width=”2″ accent_color=”#f2483e”][vc_column_text css=”.vc_custom_1667584693100{padding-top: 5% !important;}”]FetalDNA Base<\/strong> \u00e9tudie les principales anomalies du nombre de chromosomes (aneuplo\u00efdies<\/em>): le terme trisomie<\/strong> signifie que, pour ce chromosome particulier, 3 copies sont observ\u00e9es au lieu de 2, tandis que le terme monosomie signifie que le chromosome particulier est observ\u00e9 en une seule copie au lieu de 2.<\/p>\n

Le niveau FetalDNA Base<\/strong> \u00e9tudie sp\u00e9cifiquement les anomalies du chromosome 21<\/strong> (syndrome de Down<\/strong>), du chromosome 18<\/strong> (syndrome d’Edward<\/strong>) et du chromosome 13<\/strong> (syndrome de Patau<\/strong>), il repr\u00e9sente le d\u00e9passement des tests combin\u00e9s traditionnels inclus dans les d\u00e9pistages du premier trimestre (par exemple Bi-test , Tri-test, etc.)<\/p>\n

C’est le test recommand\u00e9 par toutes les Directives et par les Soci\u00e9t\u00e9s Scientifiques ; selon les indications officielles du Minist\u00e8re de la Sant\u00e9, le test pr\u00e9natal FetalDNA BASE<\/strong> doit \u00eatre ajout\u00e9 \u00e0 l’\u00e9tude \u00e9chographique de la clart\u00e9 nucale.<\/p>\n

Cet examen a des co\u00fbts extr\u00eamement faibles pour le patient et une vitesse de r\u00e9ponse \u00e9lev\u00e9e.<\/strong><\/p>\n

Le sexe f\u0153tal peut \u00e9galement \u00eatre fourni sur demande, mais PAS les anomalies chromosomiques sexuelles.<\/em><\/p>\n

Aucune information n’est fournie sur les autres anomalies chromosomiques, notamment sexuelles.<\/em>[\/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|target:_blank” softing_vc_btn_title=”#ffffff” softing_vc_btn_bg=”#f2483e” softing_vc_btn_hvrtitle=”#f2483e” softing_vc_btn_brdclr=”#f2483e” softing_vc_btn_hvrbrdclr=”#f2483e” softing_vc_btn_hvrbg=”#ffffff”][\/vc_column_inner][vc_column_inner width=”1\/4″][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner][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 screening (FetalDNA BASE) 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_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row 0=”” full_width=”stretch_row_content” softing_row_prepad=”ptb-30″ css=”.vc_custom_1641403975693{background-color: rgba(242,72,62,0.41) !important;*background-color: rgb(242,72,62) !important;}”][vc_column 0=””][vc_custom_heading text=”Afin d’\u00e9tudier d’autres alt\u00e9rations chromosomiques et g\u00e9n\u00e9tiques, il est sugg\u00e9r\u00e9 de choisir des tests NIPT plus avanc\u00e9s:” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes”][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/6″]

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FETALDNA
\nBASE PLUS<\/h4>\n

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FETALDNA BASE PLUS + 90 MICRODELEZIONI<\/h4>\n

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FETALDNA CARIOTIPO<\/h4>\n

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FETALDNA CARIOTIPO PLUS<\/h4>\n

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FETALDNA TOTAL SCREEN<\/h4>\n

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MALATTIE MONOGENICHE<\/h4>\n

<\/h4><\/div><\/div>[\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row 0=”” full_width=”stretch_row_content” css=”.vc_custom_1641403916348{padding-top: 3% !important;padding-bottom: 3% !important;}”][vc_column 0=””][vc_custom_heading text=”Tableau comparatif” font_container=”tag:h2|text_align:center|color:%23f2483e” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

Si vous vous souvenez \u00e0 quel point il est riche, il est n\u00e9, donc il est toujours en vie.<\/em><\/p>\n

[\/vc_column_text][vc_single_image source=”external_link” external_img_size=”small” alignment=”center” custom_src=”https:\/\/www.fetaldna.it\/img\/01_TableauComparatif_FetalDNA_Base_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_1641815422294{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_1641815492985{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 Base” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text] Le niveau FetalDNA Base \u00e9tudie les anomalies chromosomiques les plus courantes (aneuplo\u00efdies). [\/vc_column_text][vc_row_inner softing_row_prepad=”ptb-30″][vc_column_inner width=”1\/3″][vc_custom_heading text=”Syndrome de Down” font_container=”tag:h4|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1647382272356{border-top-width: 2px !important;border-right-width: 2px !important;border-bottom-width: 2px !important;border-left-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-9767","page","type-page","status-publish","hentry"," c-blog-1-item nt-post-class"],"yoast_head":"\nNIPT - FetalDNA Base - mini iNIPT - Altamedica Roma<\/title>\n<meta name=\"description\" content=\"Test NIPT base per individuare le 3 principali trisomie (cromosoma 13, 18 e 21). 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