Persistent Mullerian duct syndrome in two brothers from a Saudi family with a homozygous variant in the AMHR2 gene

Persistent Mullerian duct syndrome (PMDS) is a rare disease characterized by normal virilization and XY genotype including failure of Mullerian duct regression. In this article, we report two cases of PMDS in Saudi patients with a pathogenic homozygous variant in the AMHR2 gene and review the litera...

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Bibliographic Details
Main Authors: Adnan Al Shaikh, Bader Shirah
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Saudi Journal for Health Sciences
Subjects:
Online Access:http://www.saudijhealthsci.org/article.asp?issn=2278-0521;year=2020;volume=9;issue=3;spage=253;epage=256;aulast=Al