Abstract
Blind-ending bifid ureter is an extremely rare congenital anomaly. The authors report on a 13-year-old boy who presented with a previous diagnosis of right duplicated ureter and who had undergone a bilateral ureteroneocystos-tomy for vesicoureteral reflux in another clinic. The revision showed right blind-ending bifid ureter. The embryology, clinic and treatment of this anomaly is discussed.
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R. Karabulut
R. Karabulut, M.D. Gezegen Sokak No:1/10 06670 GOP Çankaya Ankara, Turkey Tel.: +90 312 2026210 Fax: +90 312 2230528 E-mail: [email protected]