Congenital urethrorectal fistula is a rare medical condition that affects the urinary and digestive systems. This condition occurs when an abnormal connection forms between the urethra, which is the tube that carries urine from the bladder, and the rectum, which is the lower part of the digestive system.
Although the exact cause of congenital urethrorectal fistula is unknown, it is believed to be a result of abnormal development during fetal development. This condition is present at birth and can vary in severity, with some cases being more complex than others.
Signs and symptoms of congenital urethrorectal fistula may include difficulty urinating, urinary tract infections, frequent urinary tract infections, and abnormal passage of stool through the urethra. In some cases, the condition may also lead to other complications such as urinary incontinence or fecal incontinence.
It's important to note that congenital urethrorectal fistula is a complex condition that requires medical attention. If you suspect your child may have this condition, it is crucial to consult with a healthcare professional who can provide a proper diagnosis and guide you through the appropriate treatment options.
Overall, understanding congenital urethrorectal fistula can help raise awareness about this rare condition. By recognizing the signs and symptoms, individuals and healthcare providers can work together to ensure proper diagnosis and management of this condition.
Congenital urethrorectal fistula is a rare condition that affects the urinary and digestive systems. It occurs when there is an abnormal connection between the urethra and the rectum. This condition can lead to a range of symptoms, such as urinary and bowel problems, and it requires timely and appropriate treatment.
If ...
To see full information about treatment please Sign up or Log in