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

Erol Basuguy, Salih Bayram


Urethral duplication is a rare congenital malformations with multiple clinical manifestations. Here, we present a boy with hypospadiac urethral duplication and multiple congenital anomalies. The patient had additional anomalies such as posterior urethral valve, left vesicoureteral reflux and right renal agenesis. This case was discussed in terms of the type of urethral duplication and the importance of additional anomalies.


Urethral duplication; hypospadias; posterior urethral valve; vesicoureteral reflux; renal agenesis

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DOI: http://dx.doi.org/10.14534/j-pucr.2019146687


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