{"id":25351,"date":"2025-04-22T13:03:26","date_gmt":"2025-04-22T12:03:26","guid":{"rendered":"https:\/\/k2info.w.uib.no\/?p=25351"},"modified":"2025-04-22T13:03:26","modified_gmt":"2025-04-22T12:03:26","slug":"nar-familiearven-er-en-sykdom","status":"publish","type":"post","link":"https:\/\/k2info.w.uib.no\/nb_no\/2025\/04\/22\/nar-familiearven-er-en-sykdom\/","title":{"rendered":"[:no]N\u00e5r familiearven er en sykdom[:en]When family inheritance is a disease[:]"},"content":{"rendered":"<p>[:no]07mai 2025<\/p>\n<p>Sted: Litteraturhuset i Bergen \u2013 Bergen<\/p>\n<p>Tidspunkt: 08.30-09.15<\/p>\n<p>Med en gentest kan man f\u00e5 informasjon om arvelige egenskaper og sykdomsrisikoer. Slike unders\u00f8kelser er viktig for diagnostisering og behandling av sykdom. Samtidig reiser bruken av genetiske unders\u00f8kelser flere sp\u00f8rsm\u00e5l og vanskelige problemstillinger. Hvordan brukes genetiske unders\u00f8kelser p\u00e5 norske sykehus i dag? Hvilken genetisk informasjon b\u00f8r deles? Og hvem b\u00f8r ha rett til \u00e5 f\u00e5 tilgang til informasjon om arvelig sykdom i sin familie?<\/p>\n<p>Overlege Ida Wiig S\u00f8rensen fra avdeling for medisinsk genetikk ved Haukeland universitetssykehus og medlem i Bioteknologir\u00e5det, diskuterer disse sp\u00f8rsm\u00e5lene i et spennende foredrag p\u00e5 Litteraturhuset i Bergen.<\/p>\n<p><a href=\"https:\/\/www.bioteknologiradet.no\/arrangement\/nar-familiearven-er-en-sykdom\/\">https:\/\/www.bioteknologiradet.no\/arrangement\/nar-familiearven-er-en-sykdom\/<\/a><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-25232\" src=\"https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1-300x200.jpg\" alt=\"\" width=\"300\" height=\"200\" srcset=\"https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1-300x200.jpg 300w, https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1-1024x683.jpg 1024w, https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1-768x512.jpg 768w, https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1-1536x1024.jpg 1536w, https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1-624x416.jpg 624w, https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1.jpg 1920w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a>[:en]May 7, 2025<br \/>\nLocation: Litteraturhuset in Bergen \u2013 Bergen<br \/>\nTime: 08.30-09.15<\/p>\n<p>With a genetic test, you can get information about hereditary characteristics and disease risks. Such tests are important for diagnosing and treating disease. At the same time, the use of genetic tests raises several questions and difficult issues. How are genetic tests used in Norwegian hospitals today? What genetic information should be shared? And who should have the right to access information about hereditary diseases in their family?<\/p>\n<p>Senior consultant Ida Wiig S\u00f8rensen from the Department of Medical Genetics at Haukeland University Hospital and member of the Biotechnology Council, discusses these questions in an exciting lecture at Litteraturhuset in Bergen.<\/p>\n<blockquote class=\"wp-embedded-content\" data-secret=\"le2Addq4pq\"><p><a href=\"https:\/\/www.bioteknologiradet.no\/arrangement\/nar-familiearven-er-en-sykdom\/\">Frokostm\u00f8te: N\u00e5r familiearven er en sykdom<\/a><\/p><\/blockquote>\n<p><iframe loading=\"lazy\" class=\"wp-embedded-content\" sandbox=\"allow-scripts\" security=\"restricted\" style=\"position: absolute; visibility: hidden;\" title=\"&laquo;Frokostm\u00f8te: N\u00e5r familiearven er en sykdom&raquo; &#8212; Bioteknologir\u00e5det\" src=\"https:\/\/www.bioteknologiradet.no\/arrangement\/nar-familiearven-er-en-sykdom\/embed\/#?secret=QAf0SjxiOw#?secret=le2Addq4pq\" data-secret=\"le2Addq4pq\" width=\"600\" height=\"338\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\"><\/iframe><\/p>\n<p><a href=\"https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-25232\" src=\"https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1-300x200.jpg\" alt=\"\" width=\"300\" height=\"200\" srcset=\"https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1-300x200.jpg 300w, https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1-1024x683.jpg 1024w, https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1-768x512.jpg 768w, https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1-1536x1024.jpg 1536w, https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1-624x416.jpg 624w, https:\/\/k2info.w.uib.no\/files\/2025\/04\/1604406784357_1.jpg 1920w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a>[:]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>[:no]07mai 2025 Sted: Litteraturhuset i Bergen \u2013 Bergen Tidspunkt: 08.30-09.15 Med en gentest kan man f\u00e5 informasjon om arvelige egenskaper og sykdomsrisikoer. Slike unders\u00f8kelser er viktig for diagnostisering og behandling av sykdom. Samtidig reiser bruken av genetiske unders\u00f8kelser flere sp\u00f8rsm\u00e5l&hellip;<\/p>\n<p class=\"more-link-p\"><a class=\"more-link\" href=\"https:\/\/k2info.w.uib.no\/nb_no\/2025\/04\/22\/nar-familiearven-er-en-sykdom\/\">Read more &rarr;<\/a><\/p>\n","protected":false},"author":5375,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[44],"tags":[],"class_list":["post-25351","post","type-post","status-publish","format-standard","hentry","category-nyheter"],"_links":{"self":[{"href":"https:\/\/k2info.w.uib.no\/nb_no\/wp-json\/wp\/v2\/posts\/25351","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/k2info.w.uib.no\/nb_no\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/k2info.w.uib.no\/nb_no\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/k2info.w.uib.no\/nb_no\/wp-json\/wp\/v2\/users\/5375"}],"replies":[{"embeddable":true,"href":"https:\/\/k2info.w.uib.no\/nb_no\/wp-json\/wp\/v2\/comments?post=25351"}],"version-history":[{"count":1,"href":"https:\/\/k2info.w.uib.no\/nb_no\/wp-json\/wp\/v2\/posts\/25351\/revisions"}],"predecessor-version":[{"id":25352,"href":"https:\/\/k2info.w.uib.no\/nb_no\/wp-json\/wp\/v2\/posts\/25351\/revisions\/25352"}],"wp:attachment":[{"href":"https:\/\/k2info.w.uib.no\/nb_no\/wp-json\/wp\/v2\/media?parent=25351"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/k2info.w.uib.no\/nb_no\/wp-json\/wp\/v2\/categories?post=25351"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/k2info.w.uib.no\/nb_no\/wp-json\/wp\/v2\/tags?post=25351"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}