{"id":3130,"date":"2025-10-06T05:52:39","date_gmt":"2025-10-06T05:52:39","guid":{"rendered":"https:\/\/genoks.com.tr\/docs\/karyotype-amniotic-fluid-sr\/"},"modified":"2026-05-02T05:05:22","modified_gmt":"2026-05-02T05:05:22","password":"","slug":"karyotype-amniotic-fluid-sr","status":"publish","type":"docs","link":"https:\/\/genoks.com.tr\/sr\/docs\/karyotype-amniotic-fluid-sr\/","title":{"rendered":"Analiza hromozoma iz amnionske te\u010dnosti (prenatalna)"},"content":{"rendered":"

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Analiza hromozoma iz amnionske te\u010dnosti (prenatalna)<\/strong> je dijagnosti\u010dki prenatalni test koji se izvodi na fetalnim \u0107elijama iz amnionske te\u010dnosti (\u226515 nedelja). Otkriva hromozomske aneuploidije (T21, T18, T13, polni hromozom) i glavne strukturne abnormalnosti. Rizik poba\u010daja vezan za proceduru ~0.1-0.3% (Akolekar 2015). Izve\u0161taj: 7-14 dana. Uzorak: 15-20 mL amnionske te\u010dnosti pomo\u0107u amniocenteze pod ultrazvu\u010dnom kontrolom. CMA se mo\u017ee dodati za procenu mikrodelecija\/duplikacija.<\/p>\n

<\/p>\n

Amniyon S\u0131v\u0131s\u0131ndan Kromozom Analizi Nedir, Neden Yap\u0131l\u0131r?<\/strong><\/p>\n

Amniyon s\u0131v\u0131s\u0131, gebelik s\u0131ras\u0131nda fet\u00fcs\u00fcn (bebe\u011fin) etraf\u0131n\u0131 saran s\u0131v\u0131d\u0131r. Amniyon s\u0131v\u0131s\u0131, fet\u00fcs\u00fcn sa\u011fl\u0131\u011f\u0131 ve geli\u015fimi hakk\u0131nda \u00f6nemli bilgiler i\u00e7erir. Bu nedenle, amniyon s\u0131v\u0131s\u0131 analizi genellikle do\u011fumsal anomalilerin veya kal\u0131tsal hastal\u0131klar\u0131n te\u015fhisinde kullan\u0131l\u0131r.<\/p>\n

Amniyosentez ad\u0131 verilen bir i\u015flem s\u0131ras\u0131nda, gebeli\u011fin 16-20. haftalar\u0131 aras\u0131nda, bir i\u011fne kullanarak anne kar\u0131n duvar\u0131ndan amniyon s\u0131v\u0131s\u0131 \u00f6rnekleri al\u0131n\u0131r. Bu s\u0131v\u0131 \u00f6rnekleri daha sonra kromozom analizi i\u00e7in laboratuvara g\u00f6nderilir.<\/p>\n

Amniyon s\u0131v\u0131s\u0131 kromozom analizi, bebe\u011fin kromozomlar\u0131n\u0131n incelenmesine olanak tan\u0131r ve genetik hastal\u0131klar\u0131n erken te\u015fhisinde \u00f6nemli bir ara\u00e7t\u0131r. Down sendromu, Edwards sendromu, Patau sendromu gibi trizomi ad\u0131 verilen kromozom anomalileri, amniyon s\u0131v\u0131s\u0131 kromozom analizi ile tespit edilebilir. Bu test ayn\u0131 zamanda, genetik risk fakt\u00f6rlerine sahip olan annelerde veya daha \u00f6nce bir do\u011fumsal anomalisi olan ailelerde tercih edilebilir.<\/p>\n

Amniyon s\u0131v\u0131s\u0131 kromozom analizi, bir\u00e7ok genetik hastal\u0131kta erken te\u015fhis ve tedavi i\u00e7in \u00f6nemli bir ara\u00e7t\u0131r. Ancak, amniyosentez i\u015flemi 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

Prenatal Nedir? <\/strong>
\n„Prenatal test“ kelimesi,\u00a0 gebelik s\u0131ras\u0131nda yap\u0131lan t\u0131bbi testleri ifade eder. Bu testler, fet\u00fcs\u00fcn sa\u011fl\u0131\u011f\u0131 ve geli\u015fimi hakk\u0131nda bilgi sa\u011flamak i\u00e7in yap\u0131l\u0131r.<\/p>\n

Prenatal testler, ebeveynlere, doktorlara ve sa\u011fl\u0131k uzmanlar\u0131na, hamilelik s\u0131ras\u0131nda al\u0131nacak kararlar hakk\u0131nda daha fazla bilgi sa\u011flar. Ancak prenatal testlerin uygulanmas\u0131 her zaman gerekli de\u011fildir ve riskleri vard\u0131r. Bu nedenle, prenatal testlerin yap\u0131lmas\u0131 gerekip gerekmedi\u011fine ve hangi testlerin yap\u0131laca\u011f\u0131na karar vermek i\u00e7in, uzman doktorlarla detayl\u0131 bir dan\u0131\u015fma yap\u0131lmas\u0131 \u00f6nerilir.<\/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>\nAmniyon s\u0131v\u0131s\u0131 Enjekt\u00f6r i\u00e7inde (S\u0130YAH P\u0130STONLU OLMAMALIDIR)<\/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

\n

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 amnionske te\u010dnosti (prenatalna) je dijagnosti\u010dki prenatalni test koji se izvodi na fetalnim \u0107elijama iz amnionske te\u010dnosti (\u226515 nedelja). Otkriva hromozomske aneuploidije (T21, T18, T13, polni hromozom) i glavne strukturne abnormalnosti. Rizik poba\u010daja vezan za proceduru ~0.1-0.3% (Akolekar [\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":[89,90,97,99,109,120],"class_list":["post-3130","docs","type-docs","status-publish","hentry","doc_category-genoks-gdhm-genetic-tests-sr","doc_tag-amniyon-sivisindan-kromozom-analizi","doc_tag-amniyosentez","doc_tag-down-sendromu","doc_tag-edwards-sendromu","doc_tag-kromozom-analizi","doc_tag-patau-sendromu"],"aioseo_notices":[],"year_month":"2026-05","word_count":532,"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":"Amniyon S\u0131v\u0131s\u0131ndan Kromozom Analizi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/amniyon-sivisindan-kromozom-analizi\/"},{"term_name":"Amniyosentez","term_url":"https:\/\/genoks.com.tr\/docs-tag\/amniyosentez\/"},{"term_name":"Down sendromu","term_url":"https:\/\/genoks.com.tr\/docs-tag\/down-sendromu\/"},{"term_name":"Edwards sendromu","term_url":"https:\/\/genoks.com.tr\/docs-tag\/edwards-sendromu\/"},{"term_name":"Kromozom Analizi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/kromozom-analizi\/"},{"term_name":"Patau sendromu","term_url":"https:\/\/genoks.com.tr\/docs-tag\/patau-sendromu\/"}],"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