Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital condition in which a
genetic female is born with vaginal agenesis and a rudimentary to absent uterus. This …

The development of the Müllerian system and the female reproductive tract is a complex
process involving an integrated series of events with significant potential for abnormal …

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Endocrinology and Infertility is now in its Seventh Edition. In a clear, user-friendly style …

Abstract BACKGROUND: The Mayer–Rokitansky–Kuester–Hauser (MRKH) syndrome is a
malformation of the female genitals (occurring in one in 4000 female live births) as a result of …

Introduction There are several techniques for creation of a neovagina. However,
rectosigmoid segment presents the most natural substitute for vaginal tissue. Aim To …

OBJECTIVE: With an incidence of up to 5% in the general population, genital malformations
are a frequent clinical occurrence. The aim of this study was to assess whether a connection …

Mayer–Rokitansky–Küster–Hauser (MRKHA) anomaly comprises agenesis of the Müllerian
duct. The condition was first described by Mayer [1829] and by Rokitansky [1838] as …

Introduction The management of vaginal agenesis is currently determined by geographical
location and surgeon preference. The optimal treatment is unknown and the majority of …

Purpose. The purpose of this study was to assess self-reported depressive and anxiety
symptoms in adolescents with polycystic ovary syndrome (PCOS) and those with the rare …

Abstract Summary of accurate diagnosis and surgical management of vaginal anomalies.
Imperforate hymen, transverse septa, and distal vaginal agenesis present similarly with pain …