{"id":3126,"date":"2025-10-06T05:52:39","date_gmt":"2025-10-06T05:52:39","guid":{"rendered":"https:\/\/genoks.com.tr\/docs\/karyotype-amniotic-fluid-az\/"},"modified":"2026-05-02T05:05:22","modified_gmt":"2026-05-02T05:05:22","password":"","slug":"karyotype-amniotic-fluid-az","status":"publish","type":"docs","link":"https:\/\/genoks.com.tr\/az\/docs\/karyotype-amniotic-fluid-az\/","title":{"rendered":"Amniotik Mayed\u0259n Xromosom Analizi (Prenatal)"},"content":{"rendered":"

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Amniyotik Mayed\u0259n Xromosom Analizi (Prenatal)<\/strong> amniyotik mayed\u0259n (\u226515 h\u0259ft\u0259) fetal h\u00fcceyr\u0259l\u0259r \u00fcz\u0259rind\u0259 apar\u0131lan diaqnostik prenatal testdir. Xromosomal an\u00f6ploidiyalar\u0131 (T21, T18, T13, cinsiyy\u0259t xromosomu) v\u0259 b\u00f6y\u00fck struktur anomaliyalar\u0131 a\u015fkar edir. Prosedurla \u0259laq\u0259li d\u00fc\u015f\u00fck riski ~0.1-0.3% (Akolekar 2015). Hesabat: 7-14 g\u00fcn. N\u00fcmun\u0259: ultras\u0259s r\u0259hb\u0259rliyind\u0259 amniyosentez il\u0259 15-20 mL amniyotik maye. Mikrodelesyon\/duplikasyon qiym\u0259tl\u0259ndirm\u0259si \u00fc\u00e7\u00fcn CMA \u0259lav\u0259 edil\u0259 bil\u0259r.<\/p>\n

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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

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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":"

Amniyotik Mayed\u0259n Xromosom Analizi (Prenatal) amniyotik mayed\u0259n (\u226515 h\u0259ft\u0259) fetal h\u00fcceyr\u0259l\u0259r \u00fcz\u0259rind\u0259 apar\u0131lan diaqnostik prenatal testdir. Xromosomal an\u00f6ploidiyalar\u0131 (T21, T18, T13, cinsiyy\u0259t xromosomu) v\u0259 b\u00f6y\u00fck struktur anomaliyalar\u0131 a\u015fkar edir. Prosedurla \u0259laq\u0259li d\u00fc\u015f\u00fck riski ~0.1-0.3% (Akolekar 2015). Hesabat: 7-14 g\u00fcn. N\u00fcmun\u0259: [\u2026]<\/span><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"closed","template":"","meta":{"footnotes":""},"doc_category":[205],"doc_tag":[89,90,97,99,109,120],"class_list":["post-3126","docs","type-docs","status-publish","hentry","doc_category-genoks-gdhm-genetik-testler-az","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":541,"total_views":0,"reactions":{"happy":0,"normal":0,"sad":0},"author_info":{"name":"admin","author_nicename":"admin","author_url":"https:\/\/genoks.com.tr\/az\/author\/admin\/"},"doc_category_info":[{"term_name":"Genoks GDHM Genetik Testl\u0259r","term_url":"https:\/\/genoks.com.tr\/az\/docs-category\/genoks-gdhm-genetik-testler-az\/"}],"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