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由于尿酸盐转运的孤立性肾脏缺陷导致的肾性低尿酸血症。

Renal hypouricemia due to an isolated renal defect of urate transport.

作者信息

Hisatome I, Ogino K, Saito M, Miyamoto J, Hasegawa J, Kotake H, Mashiba H, Nakamoto S

机构信息

First Department of Internal Medicine, Tottori University School of Medicine, Yonago, Japan.

出版信息

Nephron. 1988;49(1):81-3. doi: 10.1159/000184991.

Abstract

A 22-year-old man was found to have low serum urate concentration (1.1-1.7 mg/dl). His urate clearance was markedly increased (26.9-35.5 ml/min) and was not decreased after administration of pyrazinamide, but was even more increased after administration of benzbromarone. No other renal tubular abnormalities were detected. The young man has one sister and two brothers. His sister also has hypouricemia and hyperuricosuria. We suggest that the present case had a genetically determined renal abnormality affecting tubular presecretory reabsorption of urate.

摘要

一名22岁男性被发现血清尿酸盐浓度较低(1.1 - 1.7mg/dl)。其尿酸清除率显著升高(26.9 - 35.5ml/min),给予吡嗪酰胺后未降低,而给予苯溴马隆后甚至进一步升高。未检测到其他肾小管异常。该青年有一个姐姐和两个兄弟。他的姐姐也有低尿酸血症和高尿酸尿症。我们认为本病例存在一种由基因决定的影响肾小管尿酸分泌前重吸收的肾脏异常。

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