{"id":1782,"date":"2025-11-12T15:21:29","date_gmt":"2025-11-12T12:21:29","guid":{"rendered":"https:\/\/fideshealth.com\/fertijin\/?page_id=1782"},"modified":"2025-11-27T09:56:46","modified_gmt":"2025-11-27T06:56:46","slug":"gebelikte-tarama-testleri","status":"publish","type":"page","link":"https:\/\/fideshealth.com\/fertijin\/gebelik-takibi-ve-dogum\/gebelikte-tarama-testleri\/","title":{"rendered":"Gebelikte Tarama Testleri"},"content":{"rendered":"\n<h2 class=\"wp-block-heading\"><strong>Gebelikte Tarama Testi Nedir?<\/strong><\/h2>\n\n\n\n<p><strong>Gebelikte tarama testleri<\/strong>, bebe\u011fin genetik ya da kromozomal bir anomaliye sahip olup olmad\u0131\u011f\u0131n\u0131 belirlemek i\u00e7in yap\u0131lan testlerdir.<br>Yumurta veya sperm kaynakl\u0131 genetik hatalar embriyoda kromozomal bozukluklara yol a\u00e7abilir. Bu durum;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Down sendromu (Trizomi 21)<\/strong><\/li>\n\n\n\n<li><strong>Edwards sendromu (Trizomi 18)<\/strong><\/li>\n\n\n\n<li><strong>Patau sendromu (Trizomi 13)<\/strong>\u00a0gibi ciddi hastal\u0131klara neden olabilir.<\/li>\n<\/ul>\n\n\n\n<p>Tarama testleri&nbsp;<strong>kesin tan\u0131 koymaz<\/strong>, yaln\u0131zca&nbsp;<strong>anomali riskini \u00f6l\u00e7er.<\/strong><br>Sonu\u00e7larda risk y\u00fcksek \u00e7\u0131karsa, doktorunuz taraf\u0131ndan ileri testler (\u00f6rne\u011fin&nbsp;<strong>amniyosentez<\/strong>&nbsp;veya&nbsp;<strong>NIPT<\/strong>) \u00f6nerilebilir.<\/p>\n\n\n\n<p><a href=\"#randevu-al\">\ud83d\udc49&nbsp;<strong>Hemen randevu al\u0131n<\/strong><\/a><\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Gebelikte Testler Nelerdir?<\/strong><\/h2>\n\n\n\n<p>Gebelik s\u00fcrecinde yap\u0131lan tarama testleri aras\u0131nda en yayg\u0131n olanlar \u015funlard\u0131r:<\/p>\n\n\n\n<ol class=\"wp-block-list\">\n<li><strong>\u0130kili Tarama Testi (Kombine Test)<\/strong>\u00a0\u2013 11\u201314. haftalarda yap\u0131l\u0131r.<\/li>\n\n\n\n<li><strong>\u00dc\u00e7l\u00fc Tarama Testi<\/strong>\u00a0\u2013 16\u201318. haftalarda yap\u0131l\u0131r.<\/li>\n\n\n\n<li><strong>D\u00f6rtl\u00fc Tarama Testi<\/strong>\u00a0\u2013 15\u201322. haftalar aras\u0131nda yap\u0131l\u0131r.<\/li>\n<\/ol>\n\n\n\n<p>Bu testler,&nbsp;<strong>anne aday\u0131ndan al\u0131nan kan \u00f6rne\u011fi<\/strong>&nbsp;ve&nbsp;<strong>ultrason \u00f6l\u00e7\u00fcmleri<\/strong>&nbsp;ile ger\u00e7ekle\u015ftirilir.<br>T\u00fcp bebek gebeliklerinde de ayn\u0131 \u015fekilde uygulan\u0131r.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Gebelikte \u0130kili Tarama Testi Nedir?<\/strong><\/h2>\n\n\n\n<p><strong>\u0130kili Tarama Testi<\/strong>, t\u00fcm gebelere \u00f6nerilen ilk tarama testidir.<br>Ama\u00e7, bebe\u011fin&nbsp;<strong>Down sendromu<\/strong>&nbsp;veya di\u011fer kromozomal anomalilere sahip olma riskini belirlemektir.<\/p>\n\n\n\n<p><strong>Nas\u0131l yap\u0131l\u0131r?<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Gebeli\u011fin\u00a0<strong>11\u201313. haftalar\u0131<\/strong>\u00a0aras\u0131nda uygulan\u0131r.<\/li>\n\n\n\n<li><strong>Ultrasonografi<\/strong>\u00a0ile bebe\u011fin ense kal\u0131nl\u0131\u011f\u0131 (<strong>NT \u00f6l\u00e7\u00fcm\u00fc<\/strong>) ve burun kemi\u011fi de\u011ferlendirilir.<\/li>\n\n\n\n<li>Anne aday\u0131ndan al\u0131nan kanda\u00a0<strong>\u03b2-HCG<\/strong>\u00a0ve\u00a0<strong>PAPP-A<\/strong>\u00a0hormon d\u00fczeylerine bak\u0131l\u0131r.<\/li>\n\n\n\n<li>Sonu\u00e7lar anne ya\u015f\u0131 ve gebelik haftas\u0131yla kar\u015f\u0131la\u015ft\u0131r\u0131larak\u00a0<strong>risk oran\u0131<\/strong>\u00a0hesaplan\u0131r.<\/li>\n<\/ul>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p>\u26a0\ufe0f&nbsp;<strong>\u0130kili test a\u00e7 veya tok karna yap\u0131labilir.<\/strong>&nbsp;Test i\u00e7in \u00f6zel bir haz\u0131rl\u0131\u011fa gerek yoktur.<\/p>\n<\/blockquote>\n\n\n\n<p><strong>Sonu\u00e7 de\u011ferlendirmesi:<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>D\u00fc\u015f\u00fck risk \u2192 Takip yeterlidir.<\/li>\n\n\n\n<li>Y\u00fcksek risk \u2192 Gerekirse\u00a0<strong>amniyosentez<\/strong>\u00a0veya\u00a0<strong>NIPT testi<\/strong>\u00a0yap\u0131labilir.<\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Gebelikte \u00dc\u00e7l\u00fc Tarama Testi Nedir?<\/strong><\/h2>\n\n\n\n<p><strong>\u00dc\u00e7l\u00fc Tarama Testi<\/strong>, Down sendromu ve Trizomi 18 gibi kromozomal bozukluklara y\u00f6nelik risk de\u011ferlendirmesi yapar.<\/p>\n\n\n\n<p><strong>Uygulama zaman\u0131:<\/strong><br>Gebeli\u011fin&nbsp;<strong>16\u201318. haftalar\u0131<\/strong>&nbsp;aras\u0131nda yap\u0131l\u0131r.<\/p>\n\n\n\n<p><strong>Nas\u0131l yap\u0131l\u0131r?<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Anneden al\u0131nan kan \u00f6rne\u011finde 3 biyokimyasal parametre \u00f6l\u00e7\u00fcl\u00fcr:\n<ul class=\"wp-block-list\">\n<li><strong>HCG (Human Chorionic Gonadotropin)<\/strong><\/li>\n\n\n\n<li><strong>AFP (Alfa-Fetoprotein)<\/strong><\/li>\n\n\n\n<li><strong>E3 (Estriol)<\/strong><\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Sonu\u00e7lar,\u00a0<strong>anne ya\u015f\u0131 ve gebelik haftas\u0131yla<\/strong>\u00a0kar\u015f\u0131la\u015ft\u0131r\u0131larak risk belirlenir.<\/li>\n<\/ul>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p>Bu test de tan\u0131 koymaz, yaln\u0131zca risk saptar.<br>Sonu\u00e7 y\u00fcksek riskliyse ileri tetkiklerle do\u011frulama yap\u0131l\u0131r.<\/p>\n<\/blockquote>\n\n\n\n<p>Son y\u0131llarda,&nbsp;<strong>\u00fc\u00e7l\u00fc testin yerini d\u00f6rtl\u00fc test<\/strong>&nbsp;almaya ba\u015flam\u0131\u015ft\u0131r \u00e7\u00fcnk\u00fc daha kapsaml\u0131 bilgi sa\u011flar.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Gebelikte D\u00f6rtl\u00fc Tarama Testi Nedir?<\/strong><\/h2>\n\n\n\n<p><strong>D\u00f6rtl\u00fc Tarama Testi<\/strong>, \u00fc\u00e7l\u00fc testin geli\u015ftirilmi\u015f ve daha g\u00fcvenilir versiyonudur.<br>Hem Down sendromu hem de Trizomi 18 ve di\u011fer do\u011fumsal kusurlara ili\u015fkin riski de\u011ferlendirir.<\/p>\n\n\n\n<p><strong>Ne zaman yap\u0131l\u0131r?<\/strong><br>Gebeli\u011fin&nbsp;<strong>15\u201322. haftalar\u0131 aras\u0131nda<\/strong>, ideal olarak&nbsp;<strong>16\u201318. haftalarda<\/strong>&nbsp;yap\u0131l\u0131r.<\/p>\n\n\n\n<p><strong>Nas\u0131l yap\u0131l\u0131r?<\/strong><br>Anneden al\u0131nan kan \u00f6rne\u011finde \u015fu 4 de\u011fer incelenir:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>HCG<\/strong><\/li>\n\n\n\n<li><strong>AFP<\/strong><\/li>\n\n\n\n<li><strong>E3 (Estriol)<\/strong><\/li>\n\n\n\n<li><strong>\u0130nhibin-A<\/strong><\/li>\n<\/ul>\n\n\n\n<p><strong>Yorumlama:<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>35 ya\u015f alt\u0131 kad\u0131nlarda Down sendromu vakalar\u0131n\u0131n yakla\u015f\u0131k %75\u2019i,<\/li>\n\n\n\n<li>35 ya\u015f \u00fcst\u00fc kad\u0131nlarda ise %85\u201390\u2019\u0131 bu testle tespit edilebilir.<\/li>\n<\/ul>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p>\u0130kili test s\u00fcresini ka\u00e7\u0131ran anne adaylar\u0131 i\u00e7in d\u00f6rtl\u00fc test \u00f6nerilir.<\/p>\n<\/blockquote>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Tarama Testleri Ne Kadar G\u00fcvenilirdir?<\/strong><\/h2>\n\n\n\n<p>Tarama testleri, genetik risklerin&nbsp;<strong>yakla\u015f\u0131k %80\u201390 oran\u0131nda<\/strong>&nbsp;tespit edilmesini sa\u011flar.<br>Ancak test sonu\u00e7lar\u0131 yaln\u0131zca&nbsp;<strong>olas\u0131l\u0131k<\/strong>&nbsp;belirtir;&nbsp;<strong>kesin tan\u0131 testi de\u011fildir.<\/strong><\/p>\n\n\n\n<p>Kesin tan\u0131 i\u00e7in a\u015fa\u011f\u0131daki ileri testler uygulanabilir:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Amniyosentez<\/strong><\/li>\n\n\n\n<li><strong>Koryon Villus Biyopsisi (CVS)<\/strong><\/li>\n\n\n\n<li><strong>Non-invaziv Prenatal Test (NIPT)<\/strong><\/li>\n<\/ul>\n\n\n\n<p>T\u00fcp bebek tedavisinde gebelik sa\u011flanm\u0131\u015fsa,&nbsp;<strong>NGS (Yeni Nesil Dizileme)<\/strong>&nbsp;gibi ileri genetik analiz y\u00f6ntemleriyle embriyo transferi \u00f6ncesinde sa\u011fl\u0131kl\u0131 embriyolar se\u00e7ilebilir.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Gebelikte Tarama Testleri Ne Zaman Yap\u0131l\u0131r?<\/strong><\/h2>\n\n\n\n<figure class=\"wp-block-table\"><table class=\"has-fixed-layout\"><thead><tr><th>Test Ad\u0131<\/th><th>Uygulama Haftas\u0131<\/th><th>Ama\u00e7<\/th><\/tr><\/thead><tbody><tr><td><strong>\u0130kili Test<\/strong><\/td><td>11\u201314. hafta<\/td><td>Down sendromu risk analizi<\/td><\/tr><tr><td><strong>\u00dc\u00e7l\u00fc Test<\/strong><\/td><td>16\u201318. hafta<\/td><td>Trizomi 18 ve Down sendromu riski<\/td><\/tr><tr><td><strong>D\u00f6rtl\u00fc Test<\/strong><\/td><td>15\u201322. hafta<\/td><td>Kapsaml\u0131 genetik tarama<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Tarama Testleri Zorunlu mudur?<\/strong><\/h2>\n\n\n\n<p>Tarama testleri&nbsp;<strong>yasal olarak zorunlu de\u011fildir<\/strong>, ancak&nbsp;<strong>t\u00fcm gebelere \u00f6nerilir.<\/strong><br>Bebe\u011fin geli\u015fim s\u00fcreci ve olas\u0131 genetik riskler hakk\u0131nda \u00f6nemli bilgiler sunar.<br>Her testin sonu\u00e7lar\u0131&nbsp;<strong>doktor taraf\u0131ndan bireysel olarak<\/strong>&nbsp;de\u011ferlendirilmelidir.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>FertiJin T\u00fcp Bebek ve Kad\u0131n Sa\u011fl\u0131\u011f\u0131 Merkezi ile Gebelik Takibi<\/strong><\/h2>\n\n\n\n<p><strong>FertiJin Kad\u0131n Sa\u011fl\u0131\u011f\u0131 ve T\u00fcp Bebek Merkezi<\/strong>,<br>gebelik s\u00fcreciniz boyunca&nbsp;<strong>ikili, \u00fc\u00e7l\u00fc ve d\u00f6rtl\u00fc tarama testleri<\/strong>,<br><strong>detayl\u0131 ultrason<\/strong>,&nbsp;<strong>\u015feker y\u00fckleme testi<\/strong>&nbsp;ve&nbsp;<strong>NST<\/strong>&nbsp;uygulamalar\u0131 ile<br>hem annenin hem de bebe\u011fin sa\u011fl\u0131\u011f\u0131n\u0131 yak\u0131ndan takip eder.<\/p>\n\n\n\n<p>\ud83d\udccd&nbsp;<strong>\u0130stanbul \/ \u015ei\u015fli<\/strong><\/p>\n\n\n\n<p><a href=\"#randevu-al\">\ud83d\udc49&nbsp;<strong>Hemen randevu al\u0131n<\/strong><\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Gebelikte Tarama Testi Nedir? Gebelikte tarama testleri, bebe\u011fin genetik ya da kromozomal bir anomaliye sahip olup olmad\u0131\u011f\u0131n\u0131 belirlemek i\u00e7in yap\u0131lan testlerdir.Yumurta veya sperm kaynakl\u0131 genetik hatalar embriyoda kromozomal bozukluklara yol a\u00e7abilir. Bu durum; Tarama testleri&nbsp;kesin tan\u0131 koymaz, yaln\u0131zca&nbsp;anomali riskini \u00f6l\u00e7er.Sonu\u00e7larda risk y\u00fcksek \u00e7\u0131karsa, doktorunuz taraf\u0131ndan ileri testler (\u00f6rne\u011fin&nbsp;amniyosentez&nbsp;veya&nbsp;NIPT) \u00f6nerilebilir. \ud83d\udc49&nbsp;Hemen randevu al\u0131n Gebelikte Testler Nelerdir? [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":1774,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-1782","page","type-page","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/pages\/1782","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/comments?post=1782"}],"version-history":[{"count":0,"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/pages\/1782\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/pages\/1774"}],"wp:attachment":[{"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/media?parent=1782"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}