Duplications of the urethra are rare, but the congenital posterior urethroperineal fistula
(CUPF) is an even rarer anomaly. CUPF resembles type II A2, Y-duplication described by …

Purpose The spectrum of male urethral duplication is heterogeneous and it includes the Y-
duplication. The malformation is rare and there is only a few case series reported in the …

Complete duplication of the bladder and urethra without other congenital anomalies is a
very rare congenital anomaly. We report the case of an 8-year-old boy with complete …

Introduction Urethral duplication is a rare and variable malformation of the urinary tract, with
non-univocal and complex management. In addition, different classification schemes have …

Aims: Report of seven children with Y-type urethral duplication (YUD). Materials and
Methods:(A) Four staged operations were performed in patients having extensive perineal …

Urethral duplication is a rare congenital abnormality with varied clinical manifestations; to
this day,< 300 cases were reported in the literature. It is affecting mainly males and is nearly …

There are numerous types of urethral duplication previously described in the literature
including a Type IIA2Y where a large ventral channel branches from the hypoplastic, dorsal …

Until this 24-year-old male was sexually active, the small dimple on his penile glans had
never required any consideration. However, persistent focal irritation during sexual …

Background Congenital urethroperineal fistula is an extremely rare anomaly in which a
second channel rises from the prostatic urethra and opens onto the perineum. This entity …

Duplication of urethra is a rare congenital anomaly. We report a case of Y-type of urethral
duplication with the accessory urethra arising from posterior urethra and opening in the …