
{"id":1032,"date":"2022-02-14T09:59:42","date_gmt":"2022-02-14T08:59:42","guid":{"rendered":"https:\/\/babyjourney.se\/?p=1032"},"modified":"2025-09-26T09:30:25","modified_gmt":"2025-09-26T07:30:25","slug":"praenatal-diagnose","status":"publish","type":"post","link":"https:\/\/webstaging.babyjourney.se\/dk\/graviditet\/fosterdiagnostik\/","title":{"rendered":"Hvad er fosterdiagnostik?"},"content":{"rendered":"<p><strong>Pr\u00e6natal diagnose er en r\u00e6kke tests og unders\u00f8gelser, der giver information om fosteret. De fleste babyer f\u00f8des sunde og raske, men ultralyd, CUB, NIPT, fostervandspr\u00f8ve og moderkagepr\u00f8ver kan fort\u00e6lle dig, om fosteret har visse abnormiteter eller sygdomme.<\/strong><\/p>\n<p>Pr\u00e6natal diagnostik er en samlet betegnelse for forskellige unders\u00f8gelser og tests, der kan udf\u00f8res under graviditeten for at opdage forskellige abnormiteter hos fosteret. Pr\u00e6natal diagnostik kan give information om abnormiteter i organerne eller fosterets genetiske sammens\u00e6tning. Den nuv\u00e6rende ultralydsteknologi kan opdage mange organabnormiteter, men ikke alle. Sammen med genetisk analyse kan vi finde frem til fosterets genetiske sammens\u00e6tning.<\/p>\n<p>Der er forskellige grunde til, at folk v\u00e6lger at f\u00e5 foretaget en fosterdiagnostik. Nogle har en familiehistorie med arvelige sygdomme og \u00f8nsker at se, om fosteret er b\u00e6rer af denne sygdom, mens andre er bekymrede og \u00f8nsker at forberede sig ved at indsamle s\u00e5 mange oplysninger som muligt. Det vigtige er at beslutte, hvordan man vil forholde sig til resultatet. Kan du acceptere en sandsynlighedsberegning, eller er du en person, der har brug for et 100 % svar? Hvad ville du g\u00f8re, hvis der blev opdaget en kromosom- og\/eller organafvigelse?<\/p>\n<p>Alle former for fosterdiagnostik er helt frivillige i Sverige, og det er i sidste ende den gravide kvindes valg, hvordan hun vil forholde sig til resultaterne.<\/p>\n<p>St\u00f8rstedelen af alle b\u00f8rn, der f\u00f8des, er sunde og raske. Kun omkring 2% f\u00f8des med en eller anden form for organmisdannelse eller kromosomafvigelse. Den mest almindelige kromosomafvigelse er trisomi 21, bedre kendt som Downs syndrom. Du har altid ret til b\u00e5de mundtlig og skriftlig information om fosterdiagnostik, lige fra de muligheder, som fosterdiagnostik kan give, til de begr\u00e6nsninger og risici, som abnormiteten kan medf\u00f8re. Hver region har sine egne retningslinjer for, hvilken type fosterdiagnostik der tilbydes.<\/p>\n<h2>Pr\u00e6natal diagnose - hvilke tests kan man lave?<\/h2>\n<p>Mange undrer sig over, hvilke metoder der bruges til fosterdiagnostik. Ud over rutinem\u00e6ssig ultralyd, som tilbydes alle i Sverige, er det almindeligt at foretage fosterdiagnostik via KUB, men der er ogs\u00e5 andre muligheder.<\/p>\n<p>- <strong>Rutinem\u00e6ssig ultralyd <\/strong>udf\u00f8res normalt af en jordemoder og finder sted omkring 19-20 uger af graviditeten og viser for eksempel, hvor l\u00e6nge en graviditet har varet. Hvis du ikke har f\u00e5et en dato if\u00f8lge ultralyden p\u00e5 tidspunktet for en KUB, fasts\u00e6ttes din forventede f\u00f8dselsdato nu. Den rutinem\u00e6ssige ultralyd viser ogs\u00e5, hvor mange fostre der er i livmoderen, der foretages organscreening, moderkagen kontrolleres, fostervandet m\u00e5les, og fosterets bev\u00e6gelser registreres.<br \/>\n- <strong>KUB <\/strong>er en kombineret ultralyds- og blodpr\u00f8ve af den gravide kvinde. Den beregner sandsynligheden for Downs syndrom og to andre kromosomafvigelser. KUB kan foretages mellem uge 11+0-13+6. Testen \u00f8ger ikke risikoen for abort.<br \/>\n- <strong>NIPT<\/strong>\u00a0indeb\u00e6rer, at der tages en blodpr\u00f8ve fra den gravide kvinde fra uge 10+0 (graviditetsuge 11). P\u00e5 den m\u00e5de kan man med stor n\u00f8jagtighed se eventuelle abnormiteter i fosterets kromosomer. Hvis du ikke ved pr\u00e6cis, hvilken uge du er i (dvs. hvis du ikke har f\u00e5et IVF eller en tidlig ultralydsscanning), er det ogs\u00e5 n\u00f8dvendigt med en ultralydsscanning for at bestemme l\u00e6ngden af din graviditet. Pr\u00f8ven vil derefter blive sendt til analyse, og du kan f\u00e5 resultater for flere kromosomer end dem, der indg\u00e5r i KUB-testen. Testen \u00f8ger ikke risikoen for abort.<br \/>\n- <strong>Fostervandspr\u00f8ve <\/strong>tilbydes, f.eks. hvis en af de ovenn\u00e6vnte metoder har vist en \u00f8get sandsynlighed for en genetisk abnormitet hos fosteret, eller hvis en af for\u00e6ldrene er b\u00e6rer af en arvelig sygdom. Sammen med moderkagetest er disse test de mest p\u00e5lidelige (n\u00e6sten 100%), og de kaldes invasive test. En tynd n\u00e5l f\u00f8res ind i livmoderen, og der tages en pr\u00f8ve af fostervandet, som sendes til analyse. Det tager ca. to uger at analysere pr\u00f8ven. Fostervandspr\u00f8ven foretages tidligst i uge 15+0. Der er en lille \u00f8get risiko for spontanabort*.<br \/>\n- <strong>Pr\u00f8ve af moderkage <\/strong>er et alternativ til fostervandspr\u00f8ve. Moderkagepr\u00f8ver kan udf\u00f8res fra uge 11+0, men det kan v\u00e6re n\u00f8dvendigt at udf\u00f8re dem senere afh\u00e6ngigt af moderkagens placering. Processen er den samme som ved en fostervandspr\u00f8ve, men pr\u00f8ven tages fra moderkagen. Det tager ca. to uger at f\u00e5 et resultat. Der er en lille \u00f8get risiko for spontanabort*.<\/p>\n<p><em>*Den \u00f8gede risiko for abort ved invasiv pr\u00f8vetagning sk\u00f8nnes at v\u00e6re mindre end 1\/200.<\/em><\/p>\n<p><a href=\"https:\/\/webstaging.babyjourney.se\/dk\/graviditet\/moderkagen\/\" target=\"_blank\" rel=\"noopener\">Er du nysgerrig efter at vide mere om moderkagen? L\u00e6s mere her!<\/a><\/p>","protected":false},"excerpt":{"rendered":"<p>Pr\u00e6natal diagnose er en r\u00e6kke tests og unders\u00f8gelser, der giver information om fosteret. De fleste babyer f\u00f8des sunde og raske, men ultralyd, CUB, NIPT, fostervandspr\u00f8ve og moderkagepr\u00f8ver kan fort\u00e6lle dig, om fosteret har visse abnormiteter eller sygdomme. Pr\u00e6natal diagnose er en samlet betegnelse...<\/p>","protected":false},"author":4,"featured_media":1031,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[8],"tags":[],"class_list":["post-1032","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-graviditet"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.0 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Vad \u00e4r Fosterdiagnostik? | Baby Journey<\/title>\n<meta name=\"description\" content=\"Fosterdiagnostik \u00e4r unders\u00f6kningar som ger information om fostret. L\u00e5t oss f\u00f6rklara vad fosterdiagnostik \u00e4r f\u00f6r n\u00e5got och n\u00e4r det beh\u00f6vs. L\u00e4s mer h\u00e4r!\" \/>\n<meta name=\"robots\" content=\"noindex, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<meta property=\"og:locale\" content=\"da_DK\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Vad \u00e4r Fosterdiagnostik? | Baby Journey\" \/>\n<meta property=\"og:description\" content=\"Fosterdiagnostik \u00e4r unders\u00f6kningar som ger information om fostret. 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