The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare condition that results from the disturbance of embryonic paramesonephric duct development, which gives rise to varying degrees of malformation of reproductive organs. It is characterized by uterovaginal aplasia with normal secondary sexual characteristics and 46,XX karyotype. We report a 15-year-old female patient with MRKH. Pelvic MRI revealed cervical and uterine agenesis with the absence of the vagina. The diagnosis was confirmed based on radiological findings. The correct clinical and radiological diagnosis of MRKH by MRI is crucial for long-term management.
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Kabashi et al. (2024) studied this question.
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