CALCIUM-OXALATE STONE DISEASE - CONGENITAL DEFECT OF METABOLISM

被引：7

作者：

HAUTMANN, R ^{[1
]}

LUTZEYER, W ^{[1
]}

机构：

[1] RHEINISCH WESTFALISCHE TH, FAC MED, DEPT UROL, D-5100 AACHEN, FED REP GER

来源：

JOURNAL OF UROLOGY | 1976年 / 116卷 / 06期

关键词：

D O I：

10.1016/S0022-5347(17)58971-5

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：

Kidney tissue enzyme patterns from patients with calcium oxalate stone disease were compared to enzyme patterns from healthy and inflamed human kidneys. In the case of oxalate stone disease there was a significantly decreased activity of the glycolytic enzyme aldolase, resulting in a cumulation of oxaloacetate and of oxalic acid. This decrease of the aldolase activity does not completely reveal the cause of calcium oxalate stones but provides a new aspect to the disease.

引用

页码：687 / 689

页数：3

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