Surgery Is Not Superior to Dilation for the Management of Vaginal Agenesis in Mayer-Rokitansky-Küster-Hauser Syndrome: A Multicenter Comparative Observational Study in 131 Patients

(Abstracted from Am J Obstet Gynecol 2018;219:281.e1–281.e9)
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare congenital condition characterized by vaginal agenesis, which impairs sexuality and has a negative impact on quality of life (QOL). Classic management of this condition is to create a cavity allowing satisfying painless penetrative intercourse.

Source: Obstetrical and Gynecological Survey - February 1, 2019 Category: OBGYN Tags: GYNECOLOGY: UROGYNECOLOGY Source Type: research