Mayer-Rokitansky-Küster-Hauser Syndrome: A Case Report

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.