RT Journal Article
SR Electronic
T1 Zinner and Mayer-Rokitansky-Küster-Hauser syndromes: when unilateral renal agenesis meets genital anomalies
JF BMJ Case Reports
JO BMJ Case Reports
FD BMJ Publishing Group Ltd
SP e229034
DO 10.1136/bcr-2018-229034
VO 12
IS 5
A1 Filipa Briosa
A1 Rita Valsassina
A1 Catarina Mira
A1 Ana Zagalo
YR 2019
UL http://casereports.bmj.com/content/12/5/e229034.abstract
AB 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.