Fanconi syndrome, renal (Fanconi-Debré-Toni syndrome)
Description | (abnormally increased renal tubular phosphate-excretion) In the blood: Phosphate (↓), calcium, sodium, chlorine, creatinine, urea, glucose, 1-25-dihydroxy-vitamin D In the urine: Phosphate (↑), urine-status and sediment (glycosuria), calcium, total protein in the 24-hour urine, (aminoaciduria), osmolality Primary renal Fanconi syndrome: Molecular-genetic evaluation possible Secondary renal Fanconi syndrome: In metabolic disorders (tyrosinemia and others), plasmocytoma, intoxication with lead, cadmium, mercury, after kidney transplants, hyperparathyroidism, glucocorticoid treatment, aminoglycoside treatment |
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