Bayram, SalihBasuguy, Erol2024-04-242024-04-2420192148-2969https://doi.org/10.14534/j-pucr.2019146687https://search.trdizin.gov.tr/yayin/detay/348629https://hdl.handle.net/11468/28045Urethral duplication is a rare congenital malformation with multiple clinical manifestations. Here, wepresent a case involving a boy with hypospadiac urethral duplication and multiple congenitalanomalies. The patient had additional anomalies including a posterior urethral valve, leftvesicoureteral reflux and right renal agenesis. This case is discussed in terms of the type of urethralduplication and the importance of additional anomalies.eninfo:eu-repo/semantics/openAccessArticle611434862910.14534/j-pucr.2019146687