CONGENITAL GLOMERULOSCLEROSIS AND NEPHROTIC SYNDROME IN 2 INFANTS - SPECULATIONS AND PATHOGENESIS

被引：22

作者：

BEALE, MG ^{[1
]}

STRAYER, DS ^{[1
]}

KISSANE, JM ^{[1
]}

ROBSON, AM ^{[1
]}

机构：

[1] WASHINGTON UNIV,SCH MED,DEPT PATHOL,ST LOUIS,MO 63130

来源：

AMERICAN JOURNAL OF DISEASES OF CHILDREN | 1979年 / 133卷 / 08期

关键词：

D O I：

10.1001/archpedi.1979.02130080082017

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

The incidental finding of hyalinized glomeruli in otherwise normal infant kidneys is referred to as congenital glomerulosclerosis. Two infants had extensive glomerulosclerosis manifested by nephrotic syndrome, severe oliguria, and progressive renal failure. Both patients were believed to have had intrauterine infections. These two cases have unequivocally identified congenital glomerulosclerosis as one of the causes of nephrotic syndrome in infancy. In addition, they suggest that extensive glomerulosclerosis in some cases may be a result of congenital infections. (Am J Dis Child 133:842-845, 1979. © 1979, American Medical Association. All rights reserved.

引用

页码：842 / 845

页数：4

共 19 条

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