Review Article
Hyperuricemia in Children and Adolescents: Present Knowledge and Future Directions
Table 2
Diseases/disorders causing hyperuricemia in children and adolescents.
| 1. Gout | 2. Chronic diseases | (a) Metabolic disease | Hypoxanthine-guanine phosphoribosyl transferase (HGPRT) deficiency | (complete, Lesch–Nyhan syndrome; partial, Kelly–Seegmiller syndrome) | Adenine phosphoribosyl transferase (APRT) deficiency | Phosphoribosylpyrophosphate (PRPP) synthetase overactivity | Myoadenylate deaminase deficiency | Glycogen storage diseases (types I, III, V, and VII) | Acyl-coenzyme A dehydrogenase deficiency | (b) Down syndrome | (c) Congenital heart disease (especially cyanotic diseases) | (d) Genetic diseases | Familial juvenile hyperuricemic nephropathy (FJHN) | 3. Acute diseases | (a) Gastroenteritis (especially Rotavirus infection) | (b) Bronchial asthma (especially on attacks) | (c) Malignant disorders (tumor lysis syndrome) | (d) Hemolytic anemia | (e) Drugs | Diuretics (thiazide) | Theophylline | Anticonvulsants (valproate and phenobarbital) | Cyclosporine | Pyrazinamide | 4. Lifestyle-related disorders | (a) Obesity | (b) Metabolic syndrome |
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