Hypospadias is a birth (congenital) defect in which the opening of the urethra is on the underside of the penis. The urethra is the tube that drains urine from the bladder. In males, the opening of the urethra is normally at the end of the penis.
Hypospadias occurs in up to 4 in 1,000 newborn boys. The cause is often unknown.
Sometimes, the condition is passed down through families.
Symptoms depend on how severe the problem is.
Most often, boys with this condition have the opening of the urethra near the tip of the penis on the underside.
More severe forms of hypospadias occur when the opening is in the middle or base of the penis. Rarely, the opening is located in or behind the scrotum.
This condition may cause a downward curve of the penis during an erection. Erections are common in infant boys.
Other symptoms include:
This problem is almost always diagnosed soon after birth during a physical exam. Imaging tests may be done to look for other congenital defects.
Infants with hypospadias should not be circumcised. The foreskin should be kept intact for use in later surgical repair.
In most cases, surgery is done before the child starts school. Today, most urologists recommend repair before the child is 18 months old. Surgery can be done as young as 4 months old. During the surgery, the penis is straightened and the opening is corrected using tissue grafts from the foreskin. The repair may require several surgeries.
Results after surgery are most often good. In some cases, more surgery is needed to correct fistulas, narrowing of the urethra, or a return of the abnormal penis curve.
Most males can have normal adult sexual activity.
Call your health care provider if your son has:
Reviewed By: Sovrin M. Shah, MD, Assistant Professor, Department of Urology, The Icahn School of Medicine at Mount Sinai, New York, NY. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.