| Literature DB >> 31061196 |
Filipa Briosa1, Rita Valsassina1, Catarina Mira2, Ana Zagalo1.
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. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: congenital disorders; infant health; paediatrics; radiology
Mesh:
Year: 2019 PMID: 31061196 PMCID: PMC6510233 DOI: 10.1136/bcr-2018-229034
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X