A Case of Mayer-Rokitansky-Küster-Hauser Syndrome with Coexisting Gonadal Dysgenesis
(2025). A Case of Mayer-Rokitansky-Küster-Hauser Syndrome with Coexisting Gonadal Dysgenesis. EKB Journal Management System, 5(2), -. doi: 10.21608/esdlj.2025.456303
. "A Case of Mayer-Rokitansky-Küster-Hauser Syndrome with Coexisting Gonadal Dysgenesis". EKB Journal Management System, 5, 2, 2025, -. doi: 10.21608/esdlj.2025.456303
(2025). 'A Case of Mayer-Rokitansky-Küster-Hauser Syndrome with Coexisting Gonadal Dysgenesis', EKB Journal Management System, 5(2), pp. -. doi: 10.21608/esdlj.2025.456303
A Case of Mayer-Rokitansky-Küster-Hauser Syndrome with Coexisting Gonadal Dysgenesis. EKB Journal Management System, 2025; 5(2): -. doi: 10.21608/esdlj.2025.456303

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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