Hypospadias is a congenital condition where the urethral opening is located on the underside of the penis rather than at the tip. It occurs in approximately 1 in 250 male births globally, making it relatively common. It is much rarer in females due to differences in urethral anatomy.
The exact cause of hypospadias is often unknown, but theories suggest it may be linked to abnormal hormonal levels during fetal development, advanced maternal age, genetic factors, or exposure to pesticides and chemicals during pregnancy.
Hypospadias is typically diagnosed at birth through a physical examination by a pediatrician. The condition is often visually apparent, especially in severe cases where the urethral opening is near the scrotum or between the penis and scrotum.
Surgical treatment for hypospadias involves two main steps: straightening the penis if it is curved and relocating the urethral opening to the tip of the penis. Tissue from the patient’s body, such as foreskin, oral mucosa, or even ear cartilage, may be used to reconstruct the urethra.
Children with hypospadias may experience psychological challenges, especially if the condition is noticeable during play or social interactions. Early surgery, ideally before the age of two, is recommended to minimize these impacts and ensure normal development.
Post-surgery care involves maintaining hygiene to prevent infections, as the surgical site is prone to bacterial contamination. A catheter is typically left in place for 5-7 days to allow the wound to heal, after which normal urination should resume.
Untreated hypospadias in adulthood can lead to complications such as difficulty urinating, urinary tract infections, and bladder enlargement due to urethral narrowing. Severe cases may require emergency procedures to drain the bladder and subsequent surgical correction.