Complete diphallia associated with features of covered exstrophy.J Pediatr Surg. 2001 Jul; 36(7):E12.JP
This report describes a 1-day-old boy with complete true diphallia associated with features of covered or pseudo-exstrophy and an anorectal malformation. The urinary bladder and rectum were single. A divided sigmoid colostomy was constructed at birth for the anorectal anomaly. Complete diphallia and its likely embryogenesis are discussed.