Zinner and Mayer-Rokitansky-Küster-Hauser syndromes: when unilateral renal agenesis meets genital anomalies
- 6 May 2019
- journal article
- research article
- Published by BMJ in BMJ Case Reports
- Vol. 12 (5), e229034
- https://doi.org/10.1136/bcr-2018-229034
Abstract
Congenital unilateral renal agenesis is a relatively frequent condition at birth diagnosed mostly incidentally. Despite the excellent prognosis, unilateral renal agenesis is associated with an increased risk of other structural abnormalities, including genital malformations. The authors present two cases of asymptomatic adolescents with known congenital unilateral renal agenesis and associated genital malformations solely diagnosed during puberty—a man with Zinner syndrome and a female with Mayer-Rokitansky-Küster-Hauser syndrome.Keywords
This publication has 6 references indexed in Scilit:
- UpToDate®Oncology Times, 2017
- Zinner syndrome—a rare developmental anomaly of the mesonephric duct diagnosed on magnetic resonance imagingRadiology Case Reports, 2016
- Mayer-Rokitansky-Kuster-Hauser Syndrome: Diagnosis with MR ImagingRadiology, 2013
- Mayer-Rokitansky-Kuster-Hauser Syndrome: Embryology, Genetics and Clinical and Surgical TreatmentISRN Obstetrics and Gynecology, 2013
- Mayer–Rokitansky–Küster–Hauser syndrome: diagnosis and managementThe Obstetrician & Gynaecologist, 2012
- Zinner syndrome: A unique triad of mesonephric duct abnormalities as an unusual cause of urinary symptoms in late adolescenceIndian Journal of Urology, 2010