{"id":32,"date":"2021-06-09T13:14:33","date_gmt":"2021-06-09T13:14:33","guid":{"rendered":"https:\/\/brca.no\/?page_id=32"},"modified":"2022-02-16T08:28:08","modified_gmt":"2022-02-16T08:28:08","slug":"brca-genfeil","status":"publish","type":"page","link":"https:\/\/brca.no\/index.php\/brca-genfeil\/","title":{"rendered":"BRCA-genfeil"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"32\" class=\"elementor elementor-32\">\n\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-d89e5dc elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"d89e5dc\" data-element_type=\"section\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-44d7b58\" data-id=\"44d7b58\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-c347ee9 elementor-widget elementor-widget-spacer\" data-id=\"c347ee9\" data-element_type=\"widget\" data-widget_type=\"spacer.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"elementor-spacer\">\n\t\t\t<div class=\"elementor-spacer-inner\"><\/div>\n\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-cc1998a elementor-widget elementor-widget-heading\" data-id=\"cc1998a\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Genfeil i BRCA1 og BRCA2<\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-e174730 elementor-widget-divider--view-line_icon elementor-view-default elementor-widget-divider--element-align-center elementor-widget elementor-widget-divider\" data-id=\"e174730\" data-element_type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t\t<div class=\"elementor-icon elementor-divider__element\">\n\t\t\t\t\t<i aria-hidden=\"true\" class=\"fas fa-dna\"><\/i><\/div>\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-1eae1ed elementor-widget elementor-widget-text-editor\" data-id=\"1eae1ed\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">Kvinner med genfeil i BRCA1 eller BRCA2 har \u00f8kt risiko for brystkreft og eggstokkreft. Genfeilen arves fra en av foreldrene. Hvis en av foreldrene har en slik genfeil, er risikoen 50% for at et barn vil arve den. Man kan testes for genfeil i disse genene dersom man selv har hatt bryst- eller eggstokkreft eller hvis det er ett eller flere tilfeller av disse krefttypene i slekta.<\/span><\/p><p><span style=\"font-weight: 400;\">For at brystkreft skal oppdages p\u00e5 et tidlig stadium tilbys kvinner med genfeil MR og mammografi av begge bryst fra 25-\u00e5rs alder. For \u00e5 hindre brystkreft kan man operere bort brystkjertelvevet i begge bryst.\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">For \u00e5 unng\u00e5 eggstokkreft er den eneste effektive metoden \u00e5 fjerne begge eggstokker og eggledere. Operasjonen anbefales fra 35-40 \u00e5rs alder og n\u00e5r man har f\u00e5tt de barna man \u00f8nsker. Inngrepet gj\u00f8res ved kikkhullsoperasjon og tar vanligvis 30-45 minutter. De fleste kan reise hjem samme dag.\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">En kvinne med genfeil i BRCA1 eller BRCA2 vil ikke n\u00f8dvendigvis utvikle kreft, men per i dag finnes det ingen metode for \u00e5 si hvem som kommer til \u00e5 f\u00e5 kreft og hvem som ikke gj\u00f8r det. Derfor er r\u00e5dene like for alle.<\/span><\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-3171f7b elementor-widget elementor-widget-spacer\" data-id=\"3171f7b\" data-element_type=\"widget\" data-widget_type=\"spacer.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"elementor-spacer\">\n\t\t\t<div class=\"elementor-spacer-inner\"><\/div>\n\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>Genfeil i BRCA1 og BRCA2 Kvinner med genfeil i BRCA1 eller BRCA2 har \u00f8kt risiko for brystkreft og eggstokkreft. Genfeilen arves fra en av foreldrene. Hvis en av foreldrene har en slik genfeil, er risikoen 50% for at et barn vil arve den. Man kan testes for genfeil i disse genene dersom man selv har [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"elementor_header_footer","meta":{"footnotes":""},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v19.10 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>BRCA-genfeil - brca.no<\/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:\/\/brca.no\/index.php\/brca-genfeil\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"BRCA-genfeil - brca.no\" \/>\n<meta property=\"og:description\" content=\"Genfeil i BRCA1 og BRCA2 Kvinner med genfeil i BRCA1 eller BRCA2 har \u00f8kt risiko for brystkreft og eggstokkreft. Genfeilen arves fra en av foreldrene. Hvis en av foreldrene har en slik genfeil, er risikoen 50% for at et barn vil arve den. 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Genfeilen arves fra en av foreldrene. Hvis en av foreldrene har en slik genfeil, er risikoen 50% for at et barn vil arve den. 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