The penis plays two important roles in males by being a pathway both for urine and semen (sperm) to leave the body. Both fluids go out through a tube called the urethra (yoo-REETH-ra), which opens at the end of the penis. Sometimes, while the baby is still in his mother’s body, this opening fails to develop completely to the end of the penis and may instead be located anywhere along the underside of the penis. This condition is called hypospadias (hi-poe-SPADE-ee-us), and it is congenital (con-GEN-it-ool), meaning that your child was born with it. Many times children with hypospadias may also have an abnormal bend of the penis shaft, and a partially developed foreskin, the fold of skin at the end of the penis. The hypospadias repair surgery will reposition the opening and give the penis a more normal appearance.
When hypospadias is corrected early, most boys have no memory of having it at all; yet even older boys usually have no problems with the surgery. Once they’ve healed, most boys have little noticeable scarring from the surgery. A successful hypospadias repair as a child should last a lifetime, including during periods of rapid penis growth during puberty.