TY - JOUR T1 - Zinner and Mayer-Rokitansky-Küster-Hauser syndromes: when unilateral renal agenesis meets genital anomalies JF - BMJ Case Reports JO - BMJ Case Reports DO - 10.1136/bcr-2018-229034 VL - 12 IS - 5 SP - e229034 AU - Filipa Briosa AU - Rita Valsassina AU - Catarina Mira AU - Ana Zagalo Y1 - 2019/05/01 UR - http://casereports.bmj.com/content/12/5/e229034.abstract N2 - 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. ER -