Congenital absence of bladder and urethra - what does this mean
Congenital absence of bladder and urethra is a rare congenital disorder that occurs when the bladder and urethra fail to form properly in the womb. it is usually caused by a genetic mutation or an environmental factor. the affected individual may experience difficulty with urination and may require surgery to create a functioning urinary system.
What happens during the disease - congenital absence of bladder and urethra
Congenital absence of bladder and urethra is caused by a genetic mutation in the embryonic development of the lower urinary tract, resulting in the lack of formation of the bladder and urethra. this mutation can be inherited from the parents or can occur spontaneously. the lack of bladder and urethra can lead to urinary incontinence, recurrent urinary tract infections, and kidney damage if left untreated.
Treatment and Medical Assistance
Main goal of the treatment: To restore bladder and urethra function.
- Surgery to reconstruct the bladder and urethra
- Antibiotic therapy for any associated infections
- Regular monitoring of kidney and bladder function
- Medications to reduce bladder spasms and relieve pain
- Physical therapy to help with bladder control
- Bladder retraining to help control urination
- Urine diversion to help manage urine flow
- Long-term follow-up care
9 Days of Hospitalization Required
29 Hours Required for Outpatient Treatment
Congenital absence of bladder and urethra - Prevention
The best way to prevent congenital absence of bladder and urethra is to ensure that pregnant women are receiving adequate prenatal care. this includes regular visits to the doctor, eating a balanced diet, avoiding alcohol and drugs, and taking prenatal vitamins. additionally, genetic counseling may be recommended for families with a history of this condition.