{"id":361,"date":"2022-02-08T11:19:08","date_gmt":"2022-02-08T10:19:08","guid":{"rendered":"https:\/\/ern-ithaca.eu\/?post_type=expert-centers&#038;p=361"},"modified":"2025-06-11T13:54:22","modified_gmt":"2025-06-11T11:54:22","slug":"ern-ithaca-brussels-center-erasme","status":"publish","type":"expert-centers","link":"https:\/\/ern-ithaca.eu\/fr\/about-us\/expert-centers\/ern-ithaca-brussels-center-erasme\/","title":{"rendered":"ERN-ITHACA \u2013 Bruxelles Centre"},"content":{"rendered":"<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"291\" height=\"173\" src=\"https:\/\/ern-ithaca.eu\/wp-content\/uploads\/2022\/02\/Erasme-Hopital-Brussels.jpeg\" alt=\"\" class=\"wp-image-363\" style=\"width:543px;height:auto\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">Centre de g\u00e9n\u00e9tique humaine \u2013 ULB<br>Service de G\u00e9n\u00e9tique M\u00e9dicale \u2013 H\u00f4pital Erasme<br>Erasme Hospital \u2013 ULB<br>Route de Lennik 808<br>1070&nbsp;BRUSSELS<br>BELGIQUE<\/p>\n\n\n\n<div class=\"wp-block-buttons is-layout-flex wp-block-buttons-is-layout-flex\">\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link wp-element-button\" href=\"https:\/\/www.erasme.ulb.ac.be\/fr\/services-de-soins\/laboratoires\/genetique\">Site web<\/a><\/div>\n<\/div>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"lead\">Plomb<\/h2>\n\n\n\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-8f761849 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-vertically-aligned-center is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:15%\">\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"600\" height=\"600\" src=\"https:\/\/ern-ithaca.eu\/wp-content\/uploads\/2022\/02\/Pr-Catheline-vilain.jpeg\" alt=\"\" class=\"wp-image-362\" srcset=\"https:\/\/ern-ithaca.eu\/wp-content\/uploads\/2022\/02\/Pr-Catheline-vilain.jpeg 600w, https:\/\/ern-ithaca.eu\/wp-content\/uploads\/2022\/02\/Pr-Catheline-vilain-300x300.jpeg 300w\" sizes=\"auto, (max-width: 600px) 100vw, 600px\" \/><\/figure>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-vertically-aligned-center is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:85%\">\n<p class=\"wp-block-paragraph\"><strong>Pr Catheline VILAIN<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>T\u00e9l\u00e9phone<\/strong>: +32 (0)2 555 64 30<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Fax<\/strong>: +32 (0)2 555 64 40<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Courrier<\/strong>:&nbsp;<a href=\"mailto:genmed@erasme.ulb.ac.be\">genmed@erasme.ulb.ac.be<\/a><\/p>\n<\/div>\n<\/div>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"scope\">Champ d'application<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">En tant que membre du R\u00e9seau europ\u00e9en de r\u00e9f\u00e9rence (ERN) ITHACA, notre centre est sp\u00e9cialis\u00e9 dans tous les syndromes se caract\u00e9risant par des anomalies du d\u00e9veloppement et\/ou une d\u00e9ficience intellectuelle (DI). Environ 1 nouveau-n\u00e9 sur 40 pr\u00e9sente une malformation cong\u00e9nitale (261 pour 10 000 f\u0153tus et nouveau-n\u00e9s selon les rapports EuroCAt), et 1 sur 40 est atteint de d\u00e9ficience intellectuelle. Par cons\u00e9quent, 3 \u00e0 5 % de toutes les naissances humaines pr\u00e9sentent ou d\u00e9velopperont une anomalie du d\u00e9veloppement, parmi lesquelles au moins 25 \u00e0 50 % sont d\u2019origine g\u00e9n\u00e9tique ou g\u00e9nomique. Cette population consid\u00e9rable repr\u00e9sente en r\u00e9alit\u00e9 la juxtaposition d\u2019un tr\u00e8s grand nombre de troubles individuellement rares pr\u00e9sentant une extr\u00eame diversit\u00e9 de causes et de ph\u00e9notypes. Le champ d\u2019action et le p\u00e9rim\u00e8tre d\u2019expertise de ce centre ITHACA comprennent :<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>plus de 5 500 syndromes dysmorphiques et anomalies cong\u00e9nitales multiples (MCA), parmi lesquels plus de 3 000 maladies monog\u00e9niques, toutes les anomalies chromosomiques (dont la plupart ne sont d\u00e9tectables qu\u2019\u00e0 l\u2019aide de technologies de puces \u00e0 ADN), les anomalies dysmorphologiques multifactorielles et sporadiques, ainsi que les embryof\u00e9topathies d\u2019origine environnementale<\/li>\n\n\n\n<li>&gt;3 000 formes monog\u00e9niques et plusieurs centaines de formes chromosomiques de d\u00e9ficience intellectuelle, associ\u00e9es ou non \u00e0 un trouble du spectre autistique (TSA)<\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"service-to-patients\"><\/h2>","protected":false},"featured_media":0,"template":"","tags":[],"country":[14],"center-status":[15],"class_list":["post-361","expert-centers","type-expert-centers","status-publish","hentry","country-belgium","center-status-full-member"],"acf":{"name-city":"Brussels Center","representative":"Pr Catheline VILAIN","latitude":"50.845540 ","longitude":"4.355710","keywords-search":""},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.7 - 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