Published October 4, 2022
| Version v1
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CLINICAL AND DIAGNOSTIC FEATURES OF HYPERANDROGENISM IN MAYER-ROCKTANSKY-KUESTER-HAUSER SYNDROME
Authors/Creators
- 1. Master's Resident Samarkand State Medical University. Samarkand, Uzbekistan
- 2. Doctor of Medical Sciences, Professor Samarkand State Medical University Samarkand, Uzbekistan
- 3. Associate Professor Samarkand State Medical University
Description
Congenital uterine-vaginal aplasia or Mayer-Rokitansky-Kuester-Hauser syndrome (MRKH) is characterized by ungrown uterine buds, cervical and vaginal aplasia, but normal or hypoplastic bilateral appendages and clinically manifests as primary amenorrhea. Patients with MRKH have a normal female phenotype and karyotype development (46, XX) and an incidence of 1 per 4,000 or 5,000 newborns
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