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Congenital nephrotic syndrome Health Article
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Definition
Congenital nephrotic syndrome is disorder passed down through families in which a baby develops protein in the urine and swelling of the body. Congenital means it is present from birth. See also: Nephrotic syndrome
Alternative Names
Nephrotic syndrome - congenital
Causes, incidence, and risk factors
Congenital nephrotic syndrome is a very rare form of nephrotic syndrome. It occurs primarily in families of Finnish origin and develops shortly after birth. It is inherited, which means it is passed down through families. Children with this disorder have an abnormal form of a protein called nephrin, which is found in the kidney.
Symptoms
Signs and tests
An ultrasound done on the pregnant mother before birth may show a larger-than-normal placenta. The placenta is the organ that develops during pregnancy to feed the developing baby. Pregnant mothers may have a screening test done during pregnancy to check for this condition. The test looks for higher-than-normal levels of alpha-fetoprotein in sample of amniotic fluid. Genetic tests should be used to confirm the diagnosis if the screening test is positive. After birth, the infant will show signs of severe fluid retention and generalized swelling. The health care provider will hear abnormal sounds when listening to the baby's heart and lungs with a stethoscope. Blood pressure may be high. There may be signs of malnutrition. A urinalysis reveals large amounts of protein and the presence of fat in the urine. Total protein in the blood may be low.
Treatment
Early and aggressive treatment is needed to control the disorder. Treatment may involve:
Fluids may be restricted to help control swelling. Removal of the kidneys, dialysis, and kidney transplant may be recommended. |
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