ARTERIOVENOZ MALFORMATSIYALARI BO'LGAN BEMORLARDA CDKN2A GENIDAGI RS7865618 POLIMORFIZMINING ALLELLARI VA GENOTIPLARINING TARQALISH CHASTOTASI

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Nashr: Jild 5 Nomeri 11 : Евразийский журнал медицинских и естественных наук
Bo'lim: Статьи
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Ташкентский педиатрический медицинский институт, Республика Узбекистан, Ташкент
info@in-academy.uz
Ташкентский педиатрический медицинский институт, Республика Узбекистан, Ташкент
info@in-academy.uz

Abstrak:

Ushbu tadqiqot miya arteriovenoz malformatsiyalari (AVM) bo'lgan bemorlarda CDKN2A genidagi rs7865618 polimorfizmining allellari va genotiplarining tarqalishini tahlil qiladi, shuningdek, uning klinik fenotiplarning rivojlanishidagi potentsial rolini baholaydi. AVMlarning ko'p faktorli tabiati va ularning muhim klinik va genetik heterojenligini hisobga olgan holda, tadqiqotga 154 respondent kiritilgan: tasdiqlangan AVMlari bo'lgan 94 bemor va 60 nazorat guruhi. Genotiplash periferik qondan DNKni ajratib olish va keyinchalik o'rganilayotgan polimorfizmni o'z ichiga olgan fragmentlarni kuchaytirish orqali amalga oshirildi.

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Эркинова , С. ., & Маджидова, Я. . (2025). ARTERIOVENOZ MALFORMATSIYALARI BO’LGAN BEMORLARDA CDKN2A GENIDAGI RS7865618 POLIMORFIZMINING ALLELLARI VA GENOTIPLARINING TARQALISH CHASTOTASI. Yevrosiyo Tibbiyot Va Tabiiy Fanlar Jurnali, 5(11), 165–172. Retrieved from https://in-academy.uz/index.php/EJMNS/article/view/66095

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