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Scholars Journal of Medical Case Reports | Volume-10 | Issue-10
Herlyn Werner Wunderlich Syndrome: A Very Rare Presentation in a Teenage Girl
Dr. Tahmina Begum, Dr. Ferdousi Begum, Dr. Nazrul Islam, Dr. Sameha Alam
Published: Oct. 16, 2022 | 260 230
DOI: 10.36347/sjmcr.2022.v10i10.011
Pages: 1034-1039
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Abstract
Background: Uterus didelphys with blind hemivagina Ipsilateral renal agenesis (Herlyn Werner Wunderlich Syndrome) is a rare congenital anomaly. The true incidence of this anomaly is unknown, but it has been reported between 0.1% and 3.8%. Another name is “Double uterus-hemivaginal-renal agenesis syndrome." Case Summary: We present the case of Uterus didelphys with hemivagina with ovarian endometrioma ē Ipsilateral renal agenesis in a 14- year-old girl. Patient was symptomatically treated. She was then referred to BSMMU on 28-02-22 for further management. Conclusion: Neglected and inappropriately managed Uterus didelphys with hemivagina with ovarian endometrioma ē Ipsilateral renal agenesis can lead to endometriosis and infertility.