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Birth defects are more common in the kidney and urinary system (urinary tract) than in any other system of the body. Defects can develop in the
Each kidney continuously produces urine, which then drains through the ureter into the bladder at a low pressure. From the bladder, urine drains through the urethra to exit the body. In males, the urethra is located in the penis. In females, the urethra ends in the vulvar area (the area of the external female genital organs). Usually, urine is free of bacteria and other infectious organisms.
A Look Inside the Urinary Tract
Complications of urinary tract defects
Urinary tract defects may
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Block or slow the flow of urine
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Allow urine to flow backwards from the bladder to the kidneys (urinary reflux)
Any birth defect that blocks or slows the flow of urine can cause urine to become stagnant, which can result in urinary tract infections (UTIs) or formation of kidney stones.
Urinary reflux usually happens when defects involve the junction
where a ureter connects to the bladder. Normally the junction allows
urine to flow only one way, from the kidneys to the bladder. Defects of
the junction can allow urine to flow backward from the bladder into the
kidney (urinary reflux). In addition, other defects that block the flow
of urine can increase the pressure in the bladder and cause urinary
reflux. Reflux can affect one side or both sides.
Urinary reflux and/or frequent infections can damage the kidneys and ureters over time. Kidney damage can cause high blood pressure and rarely kidney failure.
Severe urinary tract defects in a fetus can cause little or no
urine to be produced. The fetus's urine becomes part of the fluid that
surrounds the fetus in the uterus (called amniotic fluid). If the fetus
does not release enough urine, the amount of amniotic fluid is reduced.
If there is too little amniotic fluid, the fetus's lungs, heart, face, and limbs may develop abnormally. Severe defects can cause death while the fetus is in the womb or shortly after birth.
Symptoms
Many urinary tract defects cause no symptoms and are often
discovered only when imaging studies are done for other reasons, or
during the well-child examination. Some kidney defects do not cause problems or become known until adulthood.
When urinary tract defects do cause symptoms, children may have
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Blood in their urine (hematuria)
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Recurring symptoms of urinary tract infections
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Recurring involuntary release of urine (urinary incontinence)
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Abdominal pain, and/or vomiting due to blockage (obstruction) of urine flow
Children who have urinary obstruction are also at increased risk of significant urinary bleeding after a minor injury because the kidney is under pressure.
Diagnosis
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Before birth, prenatal ultrasonography and blood tests
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After birth, imaging tests and sometimes cystoscopy
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Sometimes voiding cystourethrography
Before birth, urinary tract defects are often discovered by doctors during routine prenatal ultrasonography or other routine screening tests for hereditary disorders.
After birth, if doctors suspect a child has a urinary defect, they typically do imaging tests such as ultrasonography, computed tomography (CT), nuclear scans, and magnetic resonance imaging (MRI). Sometimes, doctors do intravenous urography or cystoscopy.
In cystoscopy, doctors look inside the bladder and urethra through a
flexible viewing tube called a cystoscope (a type of endoscope).
To diagnose certain defects of the urinary tract, doctors sometimes do a test called voiding cystourethrography
(VCUG). For voiding cystourethrography, a catheter is passed through
the urethra into the bladder, a liquid that shows up on x-rays (contrast agent) is put through the catheter, and x-rays are taken before and after the child urinates.
As children grow, these tests may be repeated at scheduled
intervals to assess how the bladder, ureters, urethra, and kidneys are
developing or functioning.
Treatment
-
Sometimes surgery
Defects that cause symptoms or those that lead to increased
pressure in the kidneys or bladder usually need to be surgically
corrected.
1 Comments
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