{"id":6779,"date":"2021-07-05T15:12:25","date_gmt":"2021-07-05T13:12:25","guid":{"rendered":"https:\/\/retina.ch\/?post_type=aktuelles&#038;p=6779"},"modified":"2021-07-06T15:36:12","modified_gmt":"2021-07-06T13:36:12","slug":"invitation-a-participer-a-lessai-clinique-therapie-genique-pour-la-retinite-pigmentaire-liee-au-chromosome-x-due-a-une-mutation-du-gene-rpgr","status":"publish","type":"aktuelles","link":"https:\/\/retina.ch\/fr\/actualites\/invitation-a-participer-a-lessai-clinique-therapie-genique-pour-la-retinite-pigmentaire-liee-au-chromosome-x-due-a-une-mutation-du-gene-rpgr\/","title":{"rendered":"Invitation \u00e0 participer \u00e0 l&rsquo;essai clinique : th\u00e9rapie g\u00e9nique pour la r\u00e9tinite pigmentaire li\u00e9e au chromosome X due \u00e0 une mutation du g\u00e8ne RPGR"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">Au nom du Dr Hoai Viet Tran, nous sommes heureux de vous faire parvenir notre invitation \u00e0 participer \u00e0 un projet de recherche de th\u00e9rapie g\u00e9nique pour la r\u00e9tinite pigmentaire li\u00e9e \u00e0 l&rsquo;X (XLRP, pour X-linked retinitis pigmentosa) qui se d\u00e9roulera \u00e0 Lausanne dans le courant de l\u2019ann\u00e9e 2021.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><strong>Titre du projet : th\u00e9rapie g\u00e9nique pour la r\u00e9tinite pigmentaire li\u00e9e au chromosome X due \u00e0 une mutation du g\u00e8ne RPGR<\/strong><\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">L&rsquo;objectif principal de l&rsquo;essai est de d\u00e9terminer si l&rsquo;injection du nouveau g\u00e8ne peut am\u00e9liorer la vision dans la maladie g\u00e9n\u00e9tique oculaire XLRP caus\u00e9e par un g\u00e8ne d\u00e9fectueux nomm\u00e9 RPGR. Cet essai de transfert de g\u00e8ne consiste \u00e0 fournir \u00e0 l&rsquo;\u0153il une version saine du g\u00e8ne RPGR, qui sera implant\u00e9 dans la r\u00e9tine par injection lors d&rsquo;une intervention chirurgicale.<br>&nbsp;<br>Apr\u00e8s l&rsquo;op\u00e9ration, vous effectuerez des visites de suivi \u00e0 l&rsquo;h\u00f4pital ophtalmique durant une p\u00e9riode de 12 mois, afin de pouvoir \u00e9valuer les cons\u00e9quences de la proc\u00e9dure sur votre vision.<br>&nbsp;<br>Toute personne atteinte de r\u00e9tinite pigmentaire li\u00e9e \u00e0 l&rsquo;X peut participer \u00e0 cet essai si elle r\u00e9pond aux crit\u00e8res ci-dessous :<\/p>\n\n\n\n<ul class=\"wp-block-list\"><li>de sexe masculin, avec un diagnostic de r\u00e9tinite pigmentaire li\u00e9e \u00e0 l&rsquo;X confirm\u00e9 par un professionnel de sant\u00e9 qualifi\u00e9<\/li><li>avec une mutation du g\u00e8ne RPGR (confirm\u00e9e par un test g\u00e9n\u00e9tique ou qui n&rsquo;a pas encore \u00e9t\u00e9 test\u00e9e)<\/li><li>\u00e2g\u00e9e de plus de 5 ans<\/li><li>avec une acuit\u00e9 visuelle corrig\u00e9e qui n&rsquo;est pas sup\u00e9rieure \u00e0 0.6 (20\/32) et qui n&rsquo;est pas inf\u00e9rieure \u00e0 0.1 (20\/200) sur l&rsquo;\u00e9chelle optom\u00e9trique pour les deux yeux.<\/li><\/ul>\n\n\n\n<p class=\"wp-block-paragraph\">Une personne atteinte de r\u00e9tinite pigmentaire li\u00e9e \u00e0 l&rsquo;X pourrait \u00eatre exclue de la participation \u00e0 l&rsquo;\u00e9tude dans les cas suivants :<\/p>\n\n\n\n<ul class=\"wp-block-list\"><li>si elle a d\u00e9j\u00e0 subi des op\u00e9rations de la r\u00e9tine, du glaucome ou de la corn\u00e9e (except\u00e9 la cataracte)<\/li><li>si elle a des ant\u00e9c\u00e9dents d&rsquo;implants occulaires, except\u00e9 un implant de lentille intraoculaire IOL<\/li><\/ul>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;Les patients int\u00e9ress\u00e9s sont pri\u00e9s de contacter :&nbsp;<a href=\"mailto:oculogenetique@fa2.ch\">oculogenetique@fa2.ch<\/a><br>Veuillez inclure une copie de votre test g\u00e9n\u00e9tique si possible.<\/p>\n\n\n\n<figure class=\"wp-block-image size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/retina.ch\/wp-content\/uploads\/2020\/11\/x-linked-vererbung.jpg\" alt=\"X-chromosomale Vererbung\" class=\"wp-image-4311\" width=\"716\" height=\"523\"\/><figcaption>Repr\u00e9sentation sch\u00e9matique de l\u2019h\u00e9ritage r\u00e9cessif li\u00e9 au chromosome X<br>(noir = malade ; blanc = sain ; noir et blanc = porteur de g\u00e8nes sains)<\/figcaption><\/figure>\n\n\n\n<hr class=\"wp-block-separator\"\/>\n\n\n\n<h3 class=\"wp-block-heading\">Pour plus d&rsquo;information<\/h3>\n\n\n\n<ul class=\"wp-block-list\"><li>Webinaire \u201c<a href=\"https:\/\/retina.ch\/agenda\/x-chromosomale-retinitis-pigmentosa\/\" target=\"_blank\" rel=\"noreferrer noopener\">La r\u00e9tinite pigmentaire li\u00e9e au Chromosome X<\/a>\u201d du 21.06.2021 avec le Dr. Hoai Viet Tran<\/li><li>Qu\u2019est-ce que c&rsquo;est la\u00a0<a href=\"https:\/\/retina.ch\/fr\/degenerescences-retiniennes\/retinite-pigmentaire\/\">r\u00e9tinite pigmentaire<\/a>\u00a0?<\/li><li><a href=\"https:\/\/retina.ch\/fr\/degenerescences-retiniennes\/x-linked\/\">H\u00e9r\u00e9dit\u00e9 li\u00e9e au chromosome X<\/a><\/li><li><a href=\"https:\/\/retina.ch\/forschung\/patientenregister\/\">Retina Suisse Registre des patients<\/a><\/li><\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Cet essai de transfert de g\u00e8ne consiste \u00e0 fournir \u00e0 l&rsquo;\u0153il une version saine du g\u00e8ne RPGR, qui sera implant\u00e9 dans la r\u00e9tine par injection lors d&rsquo;une intervention chirurgicale.<\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"_acf_changed":false,"inline_featured_image":false,"h5ap_radio_sources":[],"_FSMCFIC_featured_image_caption":"","_FSMCFIC_featured_image_nocaption":"","_FSMCFIC_featured_image_hide":"","footnotes":"","_links_to":"","_links_to_target":""},"categories":[70,62],"class_list":["post-6779","aktuelles","type-aktuelles","status-publish","hentry","category-recherche","category-retinite-pigmentaire"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Invitation \u00e0 participer \u00e0 l&#039;essai clinique : th\u00e9rapie g\u00e9nique pour la r\u00e9tinite pigmentaire li\u00e9e au chromosome X due \u00e0 une mutation du g\u00e8ne RPGR &#8226; 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