{"id":14208,"date":"2025-03-17T10:55:17","date_gmt":"2025-03-17T09:55:17","guid":{"rendered":"https:\/\/www.humangenetik-umg.de\/?p=14208"},"modified":"2025-03-17T10:55:17","modified_gmt":"2025-03-17T09:55:17","slug":"insightrp2-first-global-patient-registry-for-rp2-associated-retinitis-pigmentosa-starts-at-umg","status":"publish","type":"post","link":"https:\/\/www.humangenetik-umg.de\/en\/insightrp2-first-global-patient-registry-for-rp2-associated-retinitis-pigmentosa-starts-at-umg\/","title":{"rendered":"InsightRP2: First global patient registry for RP2-associated retinitis pigmentosa starts at UMG"},"content":{"rendered":"<div class=\"wpb-content-wrapper\">[vc_row][vc_column][mk_padding_divider size=&#8221;30&#8243;][\/vc_column][\/vc_row][vc_row][vc_column][mk_image src=&#8221;https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2025\/03\/insightrp2-visual-aktuelles-en-klein.png&#8221; image_size=&#8221;full&#8221;][\/vc_column][\/vc_row][vc_row][vc_column][mk_padding_divider size=&#8221;30&#8243;][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=&#8221;.vc_custom_1742205270411{margin-bottom: 0px !important;}&#8221;]Mutations in the <em>RP2<\/em> gene cause a specific form of retinitis pigmentosa, a group of inherited retinal disorders. The InsightRP2 registry helps clinicians and researchers better understand the genetic basis and progression of <em>RP2<\/em>-associated retinitis pigmentosa. Additionally, they can focus their research and the development of future treatment approaches on enhancing the quality of life for patients.<\/p>\n<p>The registry is organized by the Institute of Human Genetics at the University Medical Center G\u00f6ttingen.<\/p>\n<p>InsightRP2 registry is open to all patients with a confirmed diagnosis of retinitis pigmentosa associated with a causative<em> RP2<\/em> gene variant.<\/p>\n<p>To participate, please use one of the following links to the UMG registration site, depending on the patient\u2019s age: <a href=\"https:\/\/redcap.umg.eu\/surveys\/?s=RRTCPERW9EEKJXDM\" target=\"_blank\" rel=\"noopener\">adults<\/a>, <a href=\"https:\/\/redcap.umg.eu\/surveys\/?s=F9EWAPWNR7AL98LN\" target=\"_blank\" rel=\"noopener\">adolescents<\/a>, <a href=\"https:\/\/redcap.umg.eu\/surveys\/?s=E4484KKLJKCAPKN9\" target=\"_blank\" rel=\"noopener\">children<\/a>[\/vc_column_text][vc_column_text css=&#8221;.vc_custom_1742205121224{margin-bottom: 0px !important;}&#8221;]<strong>Contact:<\/strong><\/p>\n<p>Study leaders at the Institute of Human Genetics:<\/p>\n<p>Dr. med. Nina B\u00f6gershausen: <a href=\"mailto:nina.boegershausen@med.uni-goettingen.de\" target=\"_blank\" rel=\"noopener\">nina.boegershausen@med.uni-goettingen.de<\/a><br \/>\nProf. Dr. med. Bernd Wollnik: <a href=\"mailto:bernd.wollnik@med.uni-goettingen.de\" target=\"_blank\" rel=\"noopener\">bernd.wollnik@med.uni-goettingen.de<\/a>[\/vc_column_text][\/vc_column][\/vc_row]\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row][vc_column][mk_padding_divider size=&#8221;30&#8243;][\/vc_column][\/vc_row][vc_row][vc_column][mk_image src=&#8221;https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2025\/03\/insightrp2-visual-aktuelles-en-klein.png&#8221; image_size=&#8221;full&#8221;][\/vc_column][\/vc_row][vc_row][vc_column][mk_padding_divider size=&#8221;30&#8243;][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=&#8221;.vc_custom_1742205270411{margin-bottom: 0px !important;}&#8221;]Mutations in the RP2 gene cause a specific form of retinitis pigmentosa, a group of inherited retinal disorders. The InsightRP2 registry helps clinicians and researchers better understand the genetic basis and progression of RP2-associated retinitis pigmentosa. Additionally, they can focus their research and the development of future treatment [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[51,52],"tags":[],"class_list":["post-14208","post","type-post","status-publish","format-standard","hentry","category-news","category-research"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>InsightRP2: First global patient registry for RP2-associated retinitis pigmentosa starts at UMG - Institut f\u00fcr Humangenetik<\/title>\n<meta name=\"description\" content=\"InsightRP2 is the first global patient registry for RP2-associated retinitis pigmentosa, located at the Institute of Human Genetics G\u00f6ttingen.\" \/>\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.humangenetik-umg.de\/en\/insightrp2-first-global-patient-registry-for-rp2-associated-retinitis-pigmentosa-starts-at-umg\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"InsightRP2: First global patient registry for RP2-associated retinitis pigmentosa starts at UMG - 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