{"id":14171,"date":"2022-03-17T22:55:54","date_gmt":"2022-03-17T22:55:54","guid":{"rendered":"https:\/\/www.fetaldna.it\/maladies-foetales-monogeniques\/"},"modified":"2024-12-16T15:34:52","modified_gmt":"2024-12-16T15:34:52","slug":"maladies-foetales-monogeniques","status":"publish","type":"page","link":"https:\/\/www.fetaldna.it\/fr\/maladies-foetales-monogeniques\/","title":{"rendered":"Maladies f\u0153tales monog\u00e9niques"},"content":{"rendered":"

[vc_row full_width=”stretch_row” css=”.vc_custom_1642094601196{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_1642094611151{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=”Maladies f\u0153tales monog\u00e9niques” font_container=”tag:h2|text_align:center|color:%23f2483e” use_theme_fonts=”yes”][vc_column_text]<\/p>\n

Le niveau des maladies f\u0153tales monog\u00e9niques analyse les maladies sp\u00e9cifiques associ\u00e9es \u00e0 des g\u00e8nes uniques (maladies monog\u00e9niques).<\/h3>\n

[\/vc_column_text][vc_column_text css=”.vc_custom_1642094936774{padding-top: 3% !important;}”]Les troubles g\u00e9n\u00e9tiques peuvent \u00eatre h\u00e9rit\u00e9s de mani\u00e8re autosomiquedominante<\/strong>(un parent est affect\u00e9), autosomiquer\u00e9cessive<\/strong>(les deux parents sont porteurs sains) ou associ\u00e9e aux chromosomessexuels<\/strong>.<\/strong><\/strong><\/strong> Certaines maladies g\u00e9n\u00e9tiques ont \u00e9galement un d\u00e9but de novo<\/strong><\/em>, c’est-\u00e0-dire qu’elles ne sont pas transmises par les parents mais produites de mani\u00e8re fortuite.<\/p>\n

A l’exception de la b\u00eata-thalass\u00e9mie, les maladies g\u00e9n\u00e9tiques autosomiques r\u00e9cessives analys\u00e9es n’ont pas d’effet symptomatique chez le porteur sain ; pour cette raison, il existe un risque que deux sujets apparemment sains donnent naissance \u00e0 une prog\u00e9niture atteinte d’une maladie dont ils sont tous les deux porteurs.<\/p>\n

En cas de maladie g\u00e9n\u00e9tique d’apparition de novo<\/em>, l’analyse parentale ne permet pas de d\u00e9celer d’anomalies, celles-ci \u00e9tant uniquement port\u00e9es par le f\u0153tus et non pr\u00e9visibles.[\/vc_column_text][\/vc_column][\/vc_row][vc_row softing_row_prepad=”ptb-30″][vc_column][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_1642156297555{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_1642156522531{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_1642156551163{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_1642156915411{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_1642156606762{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_1642156630003{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_1642156653827{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=”Hypochondroplasie (GENE FGFR3)” font_container=”tag:h5|text_align:center” use_theme_fonts=”yes” css=”.vc_custom_1642156677034{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_1642156701146{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_1642156764059{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_1642156789308{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_1642156868035{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_1642157092444{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_1642156578780{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_1642156949099{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 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|color:%23f2483e” use_theme_fonts=”yes”][vc_single_image source=”external_link” custom_src=”https:\/\/www.fetaldna.it\/img\/08_TableauComparatif_FetalDNA_Monogeniques_FR.png”][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"

[vc_row full_width=”stretch_row” css=”.vc_custom_1642094601196{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_1642094611151{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=”Maladies f\u0153tales monog\u00e9niques” font_container=”tag:h2|text_align:center|color:%23f2483e” use_theme_fonts=”yes”][vc_column_text] Le niveau des maladies f\u0153tales monog\u00e9niques analyse les maladies sp\u00e9cifiques associ\u00e9es \u00e0 des g\u00e8nes uniques (maladies monog\u00e9niques). [\/vc_column_text][vc_column_text css=”.vc_custom_1642094936774{padding-top: 3% !important;}”]Les troubles g\u00e9n\u00e9tiques peuvent \u00eatre h\u00e9rit\u00e9s de mani\u00e8re autosomiquedominante(un…<\/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-14171","page","type-page","status-publish","hentry"," c-blog-1-item nt-post-class"],"yoast_head":"\nMaladies f\u0153tales monog\u00e9niques - FetalDNA<\/title>\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\/maladies-foetales-monogeniques\/\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Maladies f\u0153tales monog\u00e9niques - FetalDNA\" \/>\n<meta property=\"og:description\" content=\"[vc_row full_width=”stretch_row” css=”.vc_custom_1642094601196{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_1642094611151{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=”Maladies f\u0153tales monog\u00e9niques” font_container=”tag:h2|text_align:center|color:%23f2483e” use_theme_fonts=”yes”][vc_column_text] Le niveau des maladies f\u0153tales monog\u00e9niques analyse les maladies sp\u00e9cifiques associ\u00e9es \u00e0 des g\u00e8nes uniques (maladies monog\u00e9niques). [\/vc_column_text][vc_column_text css=”.vc_custom_1642094936774{padding-top: 3% !important;}”]Les troubles g\u00e9n\u00e9tiques peuvent \u00eatre h\u00e9rit\u00e9s de mani\u00e8re autosomiquedominante(un...\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.fetaldna.it\/fr\/maladies-foetales-monogeniques\/\" \/>\n<meta property=\"og:site_name\" content=\"FetalDNA\" \/>\n<meta property=\"article:modified_time\" content=\"2024-12-16T15:34:52+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=\"5 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/maladies-foetales-monogeniques\\\/\",\"url\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/maladies-foetales-monogeniques\\\/\",\"name\":\"Maladies f\u0153tales monog\u00e9niques - FetalDNA\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/#website\"},\"datePublished\":\"2022-03-17T22:55:54+00:00\",\"dateModified\":\"2024-12-16T15:34:52+00:00\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/maladies-foetales-monogeniques\\\/#breadcrumb\"},\"inLanguage\":\"fr-FR\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/maladies-foetales-monogeniques\\\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/maladies-foetales-monogeniques\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/www.fetaldna.it\\\/fr\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Maladies f\u0153tales monog\u00e9niques\"}]},{\"@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":"Maladies f\u0153tales monog\u00e9niques - FetalDNA","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\/maladies-foetales-monogeniques\/","og_locale":"fr_FR","og_type":"article","og_title":"Maladies f\u0153tales monog\u00e9niques - FetalDNA","og_description":"[vc_row full_width=”stretch_row” css=”.vc_custom_1642094601196{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_1642094611151{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=”Maladies f\u0153tales monog\u00e9niques” font_container=”tag:h2|text_align:center|color:%23f2483e” use_theme_fonts=”yes”][vc_column_text] Le niveau des maladies f\u0153tales monog\u00e9niques analyse les maladies sp\u00e9cifiques associ\u00e9es \u00e0 des g\u00e8nes uniques (maladies monog\u00e9niques). 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