Hypospadias is a birth defect (congenital condition) in which the opening of the urethra (tube through which urine drains outside from the bladder) is on the underside of the penis instead of at the tip.
There are mainly 3 types of hypospadias.
Hypospadias is a very common congenital anomaly in boys. The incidence is reported to be around 1% (1 in 100 boys).
Although the cause of hypospadias is usually unknown, these factors may be associated with the condition:
Children usually present in following ways-
Hypospadias is a correctable defect. Surgery (Urethroplasty) usually restores the normal appearance of the penis. With successful treatment of hypospadias, most males can have normal urination and reproduction.
Most infants with hypospadias are diagnosed soon after birth while still in the hospital. However, slight displacement of the urethral opening may be subtle and more difficult to identify. One should contact a pediatric surgeon if there are any concerns about the appearance of the child’s penis or if there are problems with urination (improper stream or spraying of urine).
Hypospadias repair (Urethroplasty) is done most often when boys are between 6 months and 2 years old (before going to playschool). Boys who are born with hypospadias should not be circumcised at birth. The foreskin will be needed to repair the hypospadias during surgery.
No major blood investigations are required to go ahead with the surgery. Children with proximal penile hypospadias require ultrasonography for any kidney abnormality and endocrinological workup (for cases associated with undescended testis).
Surgery for hypospadias is Urethroplasty. There are different types of urethroplasty done for various degrees of hypospadias. The surgery is done in a single operation or staged repair. Mild defects may be repaired in one procedure whereas defects associated with severe chordee (downward bending of the penis) and proximal hypospadias may need two procedures (staged repair).
If hypospadias is not treated, it can result in: