EC Gynaecology

Mini Case Study Volume 14 Issue 11 - 2025

Unveiling Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome: A Rare Genital Malformation in a 18-Year-Old with Primary Amenorrhea

IZI Zineb*, Basma Beqqali, Tlaite Oubaddi, Oumaima Mesbah, Badr Kabila, Nazik Allali, Siham El Haddad and Latifa Chat

Radiology Department, Children’s Hospital, Mohamed V University, Rabat, Morocco

*Corresponding Author: IZI Zineb, Radiology Department, Children’s Hospital, Mohamed V University, Rabat, Morocco.
Received: August 07, 2025; Published: November 04, 2025



We report the case of an 18-year-old female presenting with primary amenorrhea. Clinical examination showed normal secondary sexual characteristics. MRI revealed complete agenesis of the uterus and vagina, with normal-appearing ovaries and renal tract. These findings were consistent with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. MRI plays a key role in diagnosis and management planning of Müllerian anomalies.

 Keywords: MRKH Syndrome; Müllerian Agenesis; Primary Amenorrhea; Uterine Agenesis; Vaginal Agenesis

IZI Zineb., et al. “Unveiling Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome: A Rare Genital Malformation in a 18-Year-Old with Primary Amenorrhea”. EC Gynaecology  14.11 (2025): 01-02.

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