(Q64.5) Congenital absence of bladder and urethra

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346 088 in individuals diagnosis congenital absence of bladder and urethra confirmed
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1 928 deaths with diagnosis congenital absence of bladder and urethra
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1% mortality rate associated with the disease congenital absence of bladder and urethra

Diagnosis congenital absence of bladder and urethra is diagnosed Men are 48.17% more likely than Women

256 396

Men receive the diagnosis congenital absence of bladder and urethra

1 304 (0.5 %)

Died from this diagnosis.

100
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89 692

Women receive the diagnosis congenital absence of bladder and urethra

624 (0.7 %)

Died from this diagnosis.

Risk Group for the Disease congenital absence of bladder and urethra - Men aged 0 and Women aged 5-9

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In Men diagnosis is most often set at age 0-94
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Less common in men the disease occurs at Age 95+Less common in women the disease occurs at Age 75-95+
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In Women diagnosis is most often set at age 0-74

Disease Features congenital absence of bladder and urethra

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Absence or low individual and public risk
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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.

Clinical Pattern

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How does a doctor diagnose

  • Physical examination
  • Imaging studies such as X-rays and CT scans
  • Ultrasound
  • Cystoscopy
  • Urodynamic studies
  • Urethrocystography
  • Urethral pressure profile
  • Voiding cystourethrogram

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
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9 Days of Hospitalization Required
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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.