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Scholars Journal of Medical Case Reports | Volume-12 | Issue-09
Mayer-Rokitansky-Küster-Hauser Syndrome: A Case Report
S. Taoufiki, J. Hamdane, C. Ahmmana, I. Zouita, D. Basraoui, H. Jalal
Published: Sept. 2, 2024 |
61
62
DOI: https://doi.org/10.36347/sjmcr.2024.v12i09.002
Pages: 1518-1520
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Abstract
Mayer-Rokitansky-Küster-Hauser syndrome is a rare congenital anomaly affecting the development of the female reproductive organs. Its etiology remains undetermined, but genetic and environmental factors may play a role in its development. It comprises two types, type I isolated and type II associated with renal, vertebral or cardiac anomalies. MRI is the examination of choice to confirm the diagnosis. In the light of a Mayer-Rokitansky-Küster-Hauser observation in a 26-year-old woman who consulted us for primary amenorrhea with pelvic pain. The purpose of this case report is to raise the possibility of a diagnosis of primary amenorrhea in a young woman with normal sexual characteristics.