“…Several names have been used to refer to this pathology: congenital Y-type urethroperineal fistula, Y-type urethral duplication in a male, or Y-type congenital urethral duplication [4,5,7]. A few authors consider CUPF to be a congenital urethral duplication associated with a normal dorsal urethra and a small ventral fistula extending to the perineal skin [7], which could be categorized as a unique form or variation of urethral duplication [1,5,8]. The Effmann's classification describes different types of urethral duplication [7].…”