A rare case with multiple urinary anomalies associated with urethral duplication: Distal hypospadias, posterior urethral valve, left vesicoureteral reflux, and right renal agenesis

Urethral 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.