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Sexual Response in Women With Mayer-Rokitansky-Küster-Hauser Syndrome With a Nonsurgical Neovagina

Both, Stephanie; Kluivers, Kirsten; ten Kate-Booij, Marianne; Weijenborg, Philomeen

Obstetrical & Gynecological Survey: December 2018 - Volume 73 - Issue 12 - p 692–693
doi: 10.1097/OGX.0000000000000629

(Abstracted from Am J Obstet Gynecol 2018;219:283.e1–283.e8)

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is an uncommon congenital condition characterized by an agenesis or hypoplasia of vagina and uterus. The first-line treatment approach—nononsurgical vaginal elongation by dilation—has high success rates (90%–96%).

Outpatient Clinic of Psychosomatic Gynecology and Sexology (S.B.) and Department of Gynecology (P.W.), Leiden University Medical Centre, Leiden; Department of Gynecology, Radboud University Medical Centre, Nijmegen (K.K.); and Department of Gynecology, Erasmus Medical Centre, Rotterdam (M.t.K.-B.), The Netherlands

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