The Treatment of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome Type 1 by Mcindoe Vaginoplasty with Grafted Split-Thickness Skin in a 35-Year-Old Female: A Detailed Case-Report
B B Likhitha, Shashank N Pastay & Akshatha N Chavadi · Asian Research Journal of Gynaecology and Obstetrics · 2026
Background: Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare congenital malformation affecting phenotypically normal 46,XX females. It is characterised by primary failure of Müllerian duct development, resulting in congenital aplasia of the uterus and the upper two-thirds...
Open access
Research Article
10.9734/arjgo/2026/v9i1369