دورية أكاديمية

Case of Inherited Partial AZFa Deletion without Impact on Male Fertility

التفاصيل البيبلوغرافية
العنوان: Case of Inherited Partial AZFa Deletion without Impact on Male Fertility
المؤلفون: Baiba Alksere, Dace Berzina, Alesja Dudorova, Una Conka, Santa Andersone, Evija Pimane, Sandra Krasucka, Arita Blumberga, Aigars Dzalbs, Ieva Grinfelde, Natalija Vedmedovska, Violeta Fodina, Juris Erenpreiss
المصدر: Case Reports in Genetics, Vol 2019 (2019)
بيانات النشر: Hindawi Limited, 2019.
سنة النشر: 2019
المجموعة: LCC:Genetics
مصطلحات موضوعية: Genetics, QH426-470
الوصف: Male factor infertility accounts for 40–50% of all infertility cases. Deletions of one or more AZF region parts in chromosome Y are one of the most common genetic causes of male infertility. Usually full or partial AZF deletions, including genes involved in spermatogenesis, are associated with spermatogenic failure. Here we report a case of a Caucasian man with partial AZFa region deletion from a couple with secondary infertility. Partial AZFa deletion, involving part of USP9Y gene appears to be benign, as we proved transmission from father to son. According to our results, it is recommended to revise guidelines on markers selected for testing of AZFa region deletion, to be more selective against DDX3Y gene and exclude probably benign microdeletions involving only USP9Y gene.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2090-6544
2090-6552
Relation: https://doaj.org/toc/2090-6544; https://doaj.org/toc/2090-6552
DOI: 10.1155/2019/3802613
URL الوصول: https://doaj.org/article/db4c77e2dfda4b958b187b17b56c0370
رقم الأكسشن: edsdoj.b4c77e2dfda4b958b187b17b56c0370
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20906544
20906552
DOI:10.1155/2019/3802613