Intact spermatogenesis in an azoospermic patient with AZFa (sY84 and sY86) microdeletion and a homozygous TG12-5T variant in CFTR

Intact spermatogenesis in an azoospermic patient with AZFa (sY84 and sY86) microdeletion and a homozygous TG12-5T variant in CFTR

Background Azoospermia, the most severe form of male infertility, is categorized into two types: non-obstructive azoospermia (NOA) and obstructive azoospermia (OA), which exhibit significant genetic heterogeneity. Azoospermia factor (AZF) deletion is a common cause of NOA, whereas congenital bilater...

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Bibliographic Details
Main Authors: Yifan Sun, Beifen Zhong, Zizhou Meng, Yuxiang Zhang, Zheng Li, Chencheng Yao
Format: Article
Language:English
Published: BMC 2025-04-01
Series:Basic and Clinical Andrology
Subjects:
Azoospermia
AZFa microdeletion
Cystic fibrosis transmembrane conductance regulator gene
Spermatogenesis
Congenital bilateral absence of the vas deferens
Online Access:https://doi.org/10.1186/s12610-025-00260-7
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https://doi.org/10.1186/s12610-025-00260-7

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