| Autor: |
Manyak, Michael J., Frensilli, Frederick J., Miller, Harry C. |
| Zdroj: |
The Journal of Urology; February 1987, Vol. 137 Issue: 2 p312-314, 3p |
| Abstrakt: |
2,8-Dihydroxyadeninuria is a rare purine metabolic disorder that has been reported to have caused urolithiasis in 14 cases, mostly children. Excretion of the hydroxylated metabolites of adenine results from a deficiency of adenine phosphoribosyltransferase. The insoluble calculi have a similar chemical structure to uric acid and frequently are misdiagnosed as uric acid calculi. Management differs from that of uric acid urolithiasis. We report on an adult with 2,8-dihydroxyadenine urolithiasis in the United States. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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