{"id":3137,"date":"2025-10-06T05:52:39","date_gmt":"2025-10-06T05:52:39","guid":{"rendered":"https:\/\/genoks.com.tr\/docs\/karyotype-cvs-sr\/"},"modified":"2026-05-02T05:05:23","modified_gmt":"2026-05-02T05:05:23","password":"","slug":"karyotype-cvs-sr","status":"publish","type":"docs","link":"https:\/\/genoks.com.tr\/sr\/docs\/karyotype-cvs-sr\/","title":{"rendered":"Analiza hromozoma iz uzorka horionskih resica (CVS)"},"content":{"rendered":"

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Analiza hromozoma iz uzorka horionskih resica (CVS)<\/strong> je rani dijagnosti\u010dki prenatalni test (10-13 nedelja) na placentalnom tkivu resica, daje rezultate ranije od amniocenteze. Otkriva T21, T18, T13, aneuploidije polnih hromozoma i strukturne abnormalnosti. Rizik procedure ~0.2-0.3% (Akolekar 2015). Izve\u0161taj: 24-72h FISH\/QF-PCR; 7-14 dana pun kariotip. Ograni\u010deni placentalni mozaicizam (CPM) ~1-2%; amniocenteza za potvrdu ako je mozaicizam otkriven.<\/p>\n

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Koryonik Villus \u00d6rne\u011fi (CVS) Kromozom Analizi Nedir ?<\/strong><\/p>\n

Koryonik villus \u00f6rne\u011fi (CVS) kromozom analizi, gebeli\u011fin erken d\u00f6neminde (8-12 hafta) yap\u0131lan bir testtir. Bu test s\u0131ras\u0131nda, bebe\u011fin plasentas\u0131ndan \u00f6rnek al\u0131narak, kromozom analizi i\u00e7in laboratuvara g\u00f6nderilir.<\/p>\n

CVS kromozom analizi, genetik hastal\u0131klar\u0131n erken te\u015fhisi i\u00e7in kullan\u0131l\u0131r. Down sendromu, Edwards sendromu ve Patau sendromu gibi trizomi ad\u0131 verilen kromozom anomalileri, CVS kromozom analizi ile tespit edilebilir. Ayr\u0131ca, \u00e7e\u015fitli kal\u0131tsal hastal\u0131klar\u0131n da erken te\u015fhisinde kullan\u0131labilir.<\/p>\n

CVS, amniyon s\u0131v\u0131s\u0131 testine benzer bir testtir, ancak amniyon s\u0131v\u0131s\u0131 testinden daha erken yap\u0131l\u0131r ve sonu\u00e7lar\u0131 daha h\u0131zl\u0131 al\u0131n\u0131r. CVS testi, anne aday\u0131n\u0131n ya\u015f\u0131n\u0131n ileri oldu\u011fu veya daha \u00f6nce genetik bir hastal\u0131\u011f\u0131 olan ailelerde tercih edilebilir.<\/p>\n

CVS kromozom analizi, genellikle riskli gebeliklerde veya genetik hastal\u0131k ge\u00e7mi\u015fi olan ailelerde yap\u0131l\u0131r. Ancak, CVS testi de baz\u0131 riskleri ta\u015f\u0131r. Bu nedenle, bu test ancak doktorlar taraf\u0131ndan gerekli g\u00f6r\u00fcld\u00fc\u011f\u00fc durumlarda yap\u0131l\u0131r.<\/p>\n\n\n\n\n\n\n\n
Y\u00f6ntem :<\/strong><\/td>\nKromozom Analizi<\/td>\n<\/tr>\n
Raporlama S\u00fcresi :<\/strong><\/td>\n3-4 Hafta<\/td>\n<\/tr>\n
Prenatal\/ Postnatal:<\/strong><\/strong><\/td>\nPrenatal<\/td>\n<\/tr>\n
Gerekli Numune<\/strong>:<\/td>\nGenoks GDHM’den temin edilen transport besi yeri i\u00e7inde<\/td>\n<\/tr>\n
Saklama \/ Ta\u015f\u0131ma S\u0131cakl\u0131\u011f\u0131:<\/strong><\/td>\n+ 4C\u00b0\/ + 24C\u00b0<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

T\u00fcm genetik testlerimiz „Hasta Onam Formu“<\/strong> ve „KVKK Formu“<\/strong>nun imzalanmas\u0131n\u0131n ard\u0131ndan \u00e7al\u0131\u015f\u0131lmaya ba\u015flan\u0131r.<\/p>\n

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Detayl\u0131 Bilgi Almak \u0130\u00e7in Bize Mesaj Atabilirsiniz.<\/strong><\/p>\n\n\n\n
[contact-form-7 id=“710″ title=“genetik ba\u015fvuru“]<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

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":"

Analiza hromozoma iz uzorka horionskih resica (CVS) je rani dijagnosti\u010dki prenatalni test (10-13 nedelja) na placentalnom tkivu resica, daje rezultate ranije od amniocenteze. Otkriva T21, T18, T13, aneuploidije polnih hromozoma i strukturne abnormalnosti. Rizik procedure ~0.2-0.3% (Akolekar 2015). Izve\u0161taj: 24-72h [\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":[94,108,109,123],"class_list":["post-3137","docs","type-docs","status-publish","hentry","doc_category-genoks-gdhm-genetic-tests-sr","doc_tag-cvs","doc_tag-koryonik-villus-ornegi","doc_tag-kromozom-analizi","doc_tag-prenatal"],"aioseo_notices":[],"year_month":"2026-05","word_count":370,"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":"CVS","term_url":"https:\/\/genoks.com.tr\/docs-tag\/cvs\/"},{"term_name":"Koryonik Villus \u00d6rne\u011fi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/koryonik-villus-ornegi\/"},{"term_name":"Kromozom Analizi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/kromozom-analizi\/"},{"term_name":"Prenatal","term_url":"https:\/\/genoks.com.tr\/docs-tag\/prenatal\/"}],"aioseo_head":"\n\t\t\n\t\n\t\n\t\n\t\n\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t