Some boys are born with a birth defect where the urethra does not open at the tip of the penis. This congenital disorder forms between 8 and fourteen weeks of pregnancy. The abnormal opening can appear anywhere between the scrotum and below the end of the penis. This condition has different degrees ranging from minor to severe. The type of congenital disorder is dependent on where the opening of the urethra is located. When the urethra opens close to the head of the penis it is called subcoronal. When the opening is on the shaft of the penis it is called midshaft. If the opening is where the scrotum and penis meet, the term is penoscrotal.
This condition is referred to as hypospadias. This can result in a curved penis, issues with abnormal urine spraying and some boys need to sit to be able to urinate. In some cases, the testicle is not fully descended. If this condition is not treated it can cause issues later on such as difficulty with sexual intercourse or the inability to urinate while standing. Out of every 1,000 boys born in the United States, approximately five have this condition. This is a common birth defect among boys. The causes of this condition remain unknown. It is believed it may be caused by a combination of the mother’s environment, genes, what the mother drinks and eats and medications taken during pregnancy. For additional information please visit here.
There are numerous organizations researching the potential causes of birth defects. This has led to some important discoveries regarding this congenital disorder. There are certain common factors that increase the risks of a boy being born with this particular birth defect. The highest risks were found with mothers considered obese and above the age of 35. Women who were taking specific hormones either right before or during their pregnancy are also at a higher risk of having a baby with this birth defect. These factors are considered common denominators and not definitive proof at this point in time. There are studies currently being conducted regarding specific birth defects and the best ways to potentially prevent them. It is important for pregnant women to consult with their physicians to determine the best course of action for giving birth to a healthy child. For more details please visit this site.
This birth defect is generally diagnosed shortly after the baby is born through a physical examination. The treatment is dependent on the specifics of the defect but does require surgery to be corrected. This surgery is recommended when the boy has reached the age of between three and eighteen months. Depending on the circumstances, the surgery may be conducted in stages. The surgery may include moving the opening of the urethra into the right location, making repairs to the skin near the urethra’s opening and making corrections to the penile curve. Any baby with this condition should not be circumcised because the surgeon may require a portion of the foreskin to make the necessary repairs.