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Fanconi Syndrome
Medical Questions » Fanconi Syndrome
| Name: Fanconi Syndrome |
| Also known as: de Toni-Fanconi-Debre" Syndrome |
| Rare defect of kidney function that may be congenital (present from birth) or follow diseases such as cystinosis, glycogen storage diseases, Wilson' s disease and others. |
Causes of Fanconi Syndrome
Failure of the kidney to adequately deal with numerous chemicals and elements. |
Symptoms of Fanconi Syndrome
Abnormalities in the blood levels of calcium, phosphate, potassium and sugar. |
Tests for Fanconi Syndrome
Diagnosed by specific blood and urine tests. |
Treatment for Fanconi Syndrome
Supplements of missing calcium and potassium, increased water intake and specific dietary restrictions.
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Complications of Fanconi Syndrome of its treatment
The bone disease osteomalacia (see separate entry) and kidney failure may develop. Eye and brain abnormalities may accompany the congenital form. |
Likely Outcome of Fanconi Syndrome
Good if carefully managed. |
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