{"id":3144,"date":"2025-10-06T05:52:39","date_gmt":"2025-10-06T05:52:39","guid":{"rendered":"https:\/\/genoks.com.tr\/docs\/karyotype-fetal-blood-sr\/"},"modified":"2026-05-02T05:05:24","modified_gmt":"2026-05-02T05:05:24","password":"","slug":"karyotype-fetal-blood-sr","status":"publish","type":"docs","link":"https:\/\/genoks.com.tr\/sr\/docs\/karyotype-fetal-blood-sr\/","title":{"rendered":"Analiza hromozoma iz fetalne krvi"},"content":{"rendered":"<p><!--genoks-intro-sr:start--><\/p>\n<p><strong>Analiza hromozoma iz fetalne krvi (Kordocenteza)<\/strong> izvodi se u odabranim trudno\u0107ama (\u226518 nedelja) za brzo kariotipiranje, dijagnozu fetalne anemije\/trombocitopenije i intrauterine transfuzije. Rizik fetalnog gubitka vezan za proceduru ~1-2%, vi\u0161i od CVS\/amniocenteze. Kultura T-limfocita iz krvi pup\u010danika; rezultati za 3-7 dana. Danas se koristi u uskim indikacijama: upravljanje fetalnom anemijom, intrauterina transfuzija, brzo kariotipiranje u kasnoj gestaciji.<\/p>\n<p><!--genoks-intro-sr:end--><\/p>\n<p style=\"text-align: justify\"><strong>Fetal Kandan Kromozom Analizi Nedir ?<\/strong><\/p>\n<p style=\"text-align: justify\">Fetal kandan kromozom analizi (FKKA), gebelik d\u00f6neminde bebe\u011fin kromozomlar\u0131n\u0131n incelenmesi i\u00e7in yap\u0131lan bir testtir. Bu testte, anne karn\u0131ndaki bebe\u011fin kordon kan\u0131ndan \u00f6rnek al\u0131n\u0131r ve kromozom analizi i\u00e7in laboratuvara g\u00f6nderilir.<\/p>\n<p style=\"text-align: justify\">FKKA, amniyosentez veya koryonik villus \u00f6rne\u011fi (CVS) testi gibi di\u011fer invaziv prenatal testlerle benzer bir ama\u00e7la kullan\u0131l\u0131r. Genetik hastal\u0131klar\u0131n erken te\u015fhisi i\u00e7in yap\u0131l\u0131r ve Down sendromu, Edwards sendromu, Patau sendromu gibi trizomi ad\u0131 verilen kromozom anomalilerinin tespitinde kullan\u0131l\u0131r.<\/p>\n<p style=\"text-align: justify\">FKKA, di\u011fer invaziv prenatal testlerden farkl\u0131 olarak, anne karn\u0131ndaki bebe\u011fin kordon kan\u0131ndan \u00f6rnek al\u0131nmas\u0131 nedeniyle daha az risklidir. Ayr\u0131ca, FKKA, di\u011fer testlere g\u00f6re daha erken yap\u0131labilir (genellikle 10. haftadan itibaren), sonu\u00e7lar\u0131 daha h\u0131zl\u0131 al\u0131n\u0131r ve daha az invazivdir.<\/p>\n<table>\n<tbody>\n<tr>\n<td><strong>Y\u00f6ntem :<\/strong><\/td>\n<td>Kromozom Analizi<\/td>\n<\/tr>\n<tr>\n<td><strong>Raporlama S\u00fcresi :<\/strong><\/td>\n<td>3-4 Hafta<\/td>\n<\/tr>\n<tr>\n<td><strong><strong>Prenatal\/ Postnatal:<\/strong><\/strong><\/td>\n<td>Prenatal<\/td>\n<\/tr>\n<tr>\n<td><strong>Gerekli Numune<\/strong>:<\/td>\n<td>Heparinli T\u00fcp | heparinli Enjekt\u00f6r<\/td>\n<\/tr>\n<tr>\n<td><strong>Saklama \/ Ta\u015f\u0131ma S\u0131cakl\u0131\u011f\u0131:<\/strong><\/td>\n<td>+ 4C\u00b0\/ + 24C\u00b0<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>T\u00fcm genetik testlerimiz <strong>&#8222;Hasta Onam Formu&#8220;<\/strong> ve <strong>&#8222;KVKK Formu&#8220;<\/strong>nun imzalanmas\u0131n\u0131n ard\u0131ndan \u00e7al\u0131\u015f\u0131lmaya ba\u015flan\u0131r.<\/p>\n<hr \/>\n<p><strong>Detayl\u0131 Bilgi Almak \u0130\u00e7in Bize Mesaj Atabilirsiniz.<\/strong><\/p>\n<table>\n<tbody>\n<tr>\n<td>[contact-form-7 id=&#8220;710&#8243; title=&#8220;genetik ba\u015fvuru&#8220;]<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Genoks Genetik Hastal\u0131klar De\u011ferlendirme Merkezi T.C. Sa\u011fl\u0131k Bankanl\u0131\u011f\u0131nca denetlenen ve GHDM-SM\/06.15\/01 ruhsat numaras\u0131 ile hizmet veren sa\u011fl\u0131k kurulu\u015fudur. genoks.com.tr web sayfas\u0131nda bulunan bilgiler, genetik de\u011ferlendirme ve\/veya tan\u0131-te\u015fhis ama\u00e7l\u0131 kullan\u0131lmamal\u0131d\u0131r. T\u00fcm i\u00e7erikler bilgilendirme ama\u00e7l\u0131d\u0131r.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Analiza hromozoma iz fetalne krvi (Kordocenteza) izvodi se u odabranim trudno\u0107ama (\u226518 nedelja) za brzo kariotipiranje, dijagnozu fetalne anemije\/trombocitopenije i intrauterine transfuzije. Rizik fetalnog gubitka vezan za proceduru ~1-2%, vi\u0161i od CVS\/amniocenteze. Kultura T-limfocita iz krvi pup\u010danika; rezultati za 3-7<span class=\"excerpt-hellip\"> [\u2026]<\/span><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"closed","template":"","meta":{"footnotes":""},"doc_category":[208],"doc_tag":[90,94,100,109],"class_list":["post-3144","docs","type-docs","status-publish","hentry","doc_category-genoks-gdhm-genetic-tests-sr","doc_tag-amniyosentez","doc_tag-cvs","doc_tag-fetal-kandan-kromozom-analizi","doc_tag-kromozom-analizi"],"aioseo_notices":[],"year_month":"2026-05","word_count":328,"total_views":0,"reactions":{"happy":0,"normal":0,"sad":0},"author_info":{"name":"admin","author_nicename":"admin","author_url":"https:\/\/genoks.com.tr\/sr\/author\/admin\/"},"doc_category_info":[{"term_name":"\u0413\u0435\u043d\u0435\u0442\u0441\u043a\u0438 \u0442\u0435\u0441\u0442\u043e\u0432\u0438 Genoks GDHM","term_url":"https:\/\/genoks.com.tr\/sr\/docs-category\/genoks-gdhm-genetic-tests-sr\/"}],"doc_tag_info":[{"term_name":"Amniyosentez","term_url":"https:\/\/genoks.com.tr\/docs-tag\/amniyosentez\/"},{"term_name":"CVS","term_url":"https:\/\/genoks.com.tr\/docs-tag\/cvs\/"},{"term_name":"Fetal Kandan Kromozom Analizi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/fetal-kandan-kromozom-analizi\/"},{"term_name":"Kromozom Analizi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/kromozom-analizi\/"}],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 4.9.5.2 - aioseo.com -->\n\t<meta name=\"description\" content=\"Analiza hromozoma iz fetalne krvi (Kordocenteza) izvodi se u odabranim trudno\u0107ama (\u226518 nedelja) za brzo kariotipiranje, dijagnozu fetalne anemije\/trombocitopenije i intrauterine transfuzije. Rizik fetalnog gubitka vezan za proceduru ~1-2%, vi\u0161i od CVS\/amniocenteze. Kultura T-limfocita iz krvi pup\u010danika; rezultati za 3-7 dana. 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