[HTML][HTML] CFTR variants and renal abnormalities in males with congenital unilateral absence of the vas deferens (CUAVD): a systematic review and meta-analysis of …

H Cai, X Qing, JD Niringiyumukiza, X Zhan, D Mo… - Genetics in …, 2019 - Elsevier
Purpose CFTR variant is the main genetic contributor to congenital (unilateral/bilateral)
absence of the vas deferens (CAVD/CUAVD/CBAVD). We performed a systematic review to …

ECFS standards of care on CFTR-related disorders: Identification and care of the disorders

NJ Simmonds, KW Southern, E De Wachter… - Journal of Cystic …, 2024 - Elsevier
This is the third paper in the series providing updated information and recommendations for
people with cystic fibrosis transmembrane conductance regulator (CFTR)-related disorder …

Three cases of Klinefelter's syndrome with unilateral absence of vas deferens

EC Akinsal, N Baydilli, H Imamoglu… - Andrologia, 2017 - Wiley Online Library
Genital abnormalities such as congenital uni/bilateral absence of the vas deferens are very
rare in Klinefelter's syndrome. Here, we report three cases of Klinefelter's syndrome with …

Genetics of vas aplasia

RK Gajbhiye, S Khan, R Shah - Genetics of Male Infertility: A Case-Based …, 2020 - Springer
Congenital bilateral absence of the vas deferens (CBAVD) involves a complete or partial
defect of the Wolffian duct derivatives and is a common cause of obstructive azoospermia …

Male Infertility and Prostate Ultrasound

AM Lawrence, T Chandrasekar - Prostate Ultrasound: Current Practice …, 2015 - Springer
While infertility has become a more prominent issue in the developed world over the last two
decades, we have also gained a greater understanding of its causes, evaluation, and …

[引用][C] İnfertilite tanısı alan erkek hastalarda cftr geni sekans varyantlarının frekansı ve genotip–fenotip korelasyonunun araştırılması

M Ercan - Sağlık Bilimleri Enstitüsü