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Alport syndrome Health Article
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Definition
Alport syndrome is an inherited disorder that leads to kidney damage.
Alternative Names
Hereditary nephritis; Hematuria - nephropathy - deafness; Hemorrhagic familial nephritis; Hereditary deafness and nephropathy
Causes, incidence, and risk factors
Alport syndrome is an inherited form of kidney inflammation (nephritis). It's caused by a mutation in a gene for a protein in connective tissue, called collagen. The disorder is uncommon, and most often affects males. Women can transmit the gene for the disorder to their children, even if they have no symptoms. Risk factors include:
Symptoms
The disorder damages the tiny blood vessels in the kidneys, called glomeruli, that filter wastes. At first, there are no symptoms. Then the progressive destruction of the glomeruli leads to blood in the urine and decreases the effectiveness of the kidney's filtering system. There is a progressive loss of kidney function and a build-up of fluids and wastes in the body. In women, the disorder is usually mild, with minimal or no symptoms. In men, the symptoms are more severe and get worse faster. Symptoms include:
The condition can progress to end-stage renal disease (ESRD) at an early age (between adolescence and age 40). Note: There may be no symptoms in some cases. Symptoms of chronic kidney failure or heart failure may be present or may develop.
Signs and tests
The following tests may be done:
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