FAMILIAL RENAL HYPOURICEMIA - 2 ADDITIONAL CASES WITH URIC-ACID LITHIASIS

被引：36

作者：

FRANK, M ^{[1
]}

MANY, M ^{[1
]}

SPERLING, O ^{[1
]}

机构：

[1] ROGOFF WELCOME MED RES INST,TEL AVIV,ISRAEL

来源：

BRITISH JOURNAL OF UROLOGY | 1979年 / 51卷 / 02期

关键词：

D O I：

10.1111/j.1464-410X.1979.tb02838.x

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

Two families are reported affected with hereditary renal hypouricaemia associated with uric acid lithiasis. The propositi of both families were found also to have hyperabsorptive hypercalciuria. Based on the study of the effect of pyrazinamide and probenecid on uric acid excretion in both propositi, it is suggested that the defect in uric acid reabsorption is most probably at the presecretory site. Copyright © 1979, Wiley Blackwell. All rights reserved

引用

页码：88 / 91

页数：4

共 18 条

[1]

Atsmon A, 1963, URIC ACID LITHIASIS

[2] FAMILIAL HYPOURICEMIA DUE TO ISOLATED RENAL TUBULAR DEFECT - ATTENUATED RESPONSE OF URIC-ACID CLEARANCE TO PROBENECID AND PYRAZINAMIDE [J].