Department of Obstetrics and Gynecology II, CHU HASSAN II, FES.
World Journal of Advanced Research and Reviews, 2026, 29(02), 613-615
Article DOI: 10.30574/wjarr.2026.29.2.0329
Received on 31 December 2025; revised on 07 February 2026; accepted on 09 February 2026
Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is a rare cause of primary amenorrhea. It is characterized by congenital aplasia of the uterus and the upper two-thirds of the vagina in women with normal development of secondary sexual characteristics. The diagnosis relies mainly on magnetic resonance imaging (MRI).
We report the case of a 27-year-old woman presenting with primary amenorrhea and well-developed secondary sexual characteristics. Hormonal investigations revealed normal ovarian function and a normal gonadotropic axis. Pelvic ultrasound and MRI demonstrated complete uterine agenesis, confirming the diagnosis of MRKH syndrome.
This report highlights the importance of suspecting MRKH syndrome in young women with normal secondary sexual characteristics presenting with primary amenorrhea, regardless of its type, and emphasizes the essential role of MRI in identifying specific features of this condition.
Primary Amenorrhea; Uterovaginal Aplasia; MRI; Case Report
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Sanae Melaim, Sofia Jayi, Zineb Tazi, Yassine Belhaj, Fatime Zohra Fdili, Hikmat Chaara and Melhouf MoulayAbdelilah. Mayer–Rokitansky–Küster–Hauser Syndrome: A Case Report and Review of the Literature. World Journal of Advanced Research and Reviews, 2026, 29(02), 613-615. Article DOI: https://doi.org/10.30574/wjarr.2026.29.2.0329.
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