A baby boy in Pakistan was born with an incredibly rare medical condition known as diphallia, which means he has two working penises but no anus. According to a team of researchers who published their findings in the International Journal of Surgery Case Reports, the chances of being born with this condition are one in six million. Diphallia can present as complete or incomplete and is often associated with complex urological, gastrointestinal, or anorectal malformations.
The abstract of the study revealed that the boy’s penises were both normal-shaped, with one being slightly larger than the other at 2.5 cm and 1.5 cm in length, respectively. The boy had two separate urethral orifices, and both phalluses had normal-shaped glans with urethral openings located in the typical position. He had a single scrotum with two midline raphe and well-formed rouge. The boy was passing urine from both orifices, and an ultrasonography of his urological system showed two ureters and a single hemi bladder.
After being admitted to the hospital, the baby boy underwent surgery, and a sigmoid-divided colostomy was constructed. During the operation, the doctors also identified a congenital pouch colon. To enable the baby to pass stools, the doctors created an opening via a colonoscopy.
