Mayer-Rokitansky-Küster-Hauser Syndrome: Admission With An Atypical Chief Complaint

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital abnormality with absence of uterus, cervix and vagina, together with normal sex development and external genitalia. It’s a rare case of girls seen in every 4,000 to 10,000 births. The syndrome, usually identified during the investigation of primary amenorrhea in puberty, may have additional abnormalities, that also can cause a variety of clinical complaints. However, in the literature there is no patients diagnosed as a result of admission with complaints of micturition. Urinary incontinence is common among women but while they do not seek for medical help and while they think that it’s a natural process though the situation affects their quality of life, may delay the diagnosis of important factors that may lie beneath. For the correct identification of these patients in clinical practice all female patients admitted to the clinic for any reason incontinence should be noted by physicians