Arslan, SerkanAydoğdu, BahattinZeytun, HikmetBasuguy, ErolOkur, Mehmet HanifiArslan, Mehmet Şerif2024-04-242024-04-2420152148-2969https://search.trdizin.gov.tr/yayin/detay/197509https://hdl.handle.net/11468/27454Urethral duplication is a rare congenital anomaly, usually found with multiple anatomical variants. In this article was presented a case of urethral duplication in an 8-month-old male child. The malformation was characterized by the presence of continent hypospadic and normal apical urethra. Retrograde urethrogram through both urethral tracts simultaneously revealed the malformation as Effmann Type II A-2. The accessory ventral urethra was excised without complicationeninfo:eu-repo/semantics/openAccessArticle211924197509