Mayer-Rokitansky-Kuster-Hauser syndrome
MONDO:0017771Spectrum of Mullerian duct anomalies characterized by congenital aplasia of the uterus and upper 2/3 of the vagina in otherwise phenotypically normal females. It can be classified as either MRKH syndrome type 1 (corresponding to isolated utero-vaginal aplasia) or MRKH syndrome type 2 (utero-vaginal aplasia associated with other malformations).
Also known as: MRKH, MRKH syndrome, Mayer-Rokitansky-Küster-Hauser Syndrome, Mullerian aplasia/dysgenesis, Rokitansky Kuster Hauser syndrome, Rokitansky syndrome, Mayer-Rokitansky-Küster-Hauser syndrome
10 clinical trials for this condition and its sub-types.
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How do women with MRKH syndrome fare after a decade?
Knowledge-focused CompletedThis study looks at how the quality of life changes over time for young women with MRKH syndrome, a condition where the uterus and upper vagina are underdeveloped. Researchers followed 25 women who took part in an earlier study, asking them to fill out questionnaires about their …
Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:58 UTC
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Study explores life quality after vaginal aplasia treatments
Knowledge-focused CompletedThis completed study looked at 138 women with Rokitansky syndrome, a condition where the vagina and uterus are underdeveloped. Researchers compared quality of life and sexual health in women who had surgery versus those who used vaginal dilation. The goal was to see which approac…
Phase: NA • Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused
Last updated Jun 26, 2026 13:23 UTC