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家族性孤立性肾小管尿酸尿症所致低尿酸血症。采用吡嗪酰胺-丙磺舒联合试验进行评估。

Hypouricemia due to familial isolated renal tubular uricosuria. Evaluation with the combined pyrazinamide-probenecid test.

作者信息

Gafter U, Zuta A, Frydman M, Lewinski U H, Levi J

机构信息

Department of Nephrology, Hasharon Hospital, Petah Tiqva, Israel.

出版信息

Miner Electrolyte Metab. 1989;15(5):309-14.

PMID:2811790
Abstract

A Jewish Iraqi woman with familial isolated renal tubular uricosuria, urate clearance of 60.5 +/- 5.7 ml/min and hypouricemia of 1.0 +/- 0.2 mg/dl is described. The combined pyrazinamide-probenecid test suggested a presecretory defect in urate reabsorption. Four offspring were moderately affected. This family represents the sixth Jewish Iraqi family with familial isolated presecretory uricosuria, and emphasizes the marked prevalence of this disease among the Iraqi Jewish population. Since the inheritance of the presecretory defect is autosomal recessive, we suggest that this family is an example of pseudodominant transmission. The combined pyrazinamide-probenecid test may cause a reduction in glomerular filtration rate and filtered load of urate and thereby affect urinary excretion rate of urate in patients with urate wasting.

摘要

本文描述了一名患有家族性孤立性肾小管尿酸尿症的伊拉克犹太女性,其尿酸清除率为60.5±5.7ml/min,低尿酸血症为1.0±0.2mg/dl。吡嗪酰胺-丙磺舒联合试验提示尿酸重吸收存在分泌前缺陷。四个后代受到中度影响。这个家族是第六个患有家族性孤立性分泌前尿酸尿症的伊拉克犹太家族,强调了这种疾病在伊拉克犹太人群中的显著患病率。由于分泌前缺陷的遗传方式为常染色体隐性遗传,我们认为这个家族是假显性遗传的一个例子。吡嗪酰胺-丙磺舒联合试验可能会导致肾小球滤过率和尿酸滤过负荷降低,从而影响尿酸排泄型患者的尿酸尿排泄率。

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