A Case of Mayer-Rokitansky-Küster-Hauser Syndrome with Coexisting Gonadal Dysgenesis | ||
| Egyptian Society of Diabetes and Lipidology Journal | ||
| Volume 5, Issue 2, October 2025 PDF (906.99 K) | ||
| Document Type: Case Report | ||
| DOI: 10.21608/esdlj.2025.456303 | ||
| Abstract | ||
| Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital disorder characterized by agenesis or aplasia of the uterus and upper part of the vagina in a phenotypically and karyotypically normal female (46,XX). Patients present with primary amenorrhea and normal secondary sexual characteristics. Ovarian anomalies with MRKH are rare and only found in ~ 5–10% of cases (21 reported cases). These patients present with both primary amenorrhea and absent secondary sexual characteristics. | ||
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