HEREDITARY ANGIO-OEDEMA TREATED WITH E-AMINOCAPROIC ACID

被引：46

作者：

CHAMPION, RH

LACHMANN, PJ

机构：

[1] Department of Dermatology, Addenbrooke's Hospital, Immunology Division, Department of Pathology

来源：

BRITISH JOURNAL OF DERMATOLOGY | 1969年 / 81卷 / 10期

关键词：

D O I：

10.1111/j.1365-2133.1969.tb15938.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

SUMMARY.— Two brothers with hereditary angio‐oedema have been studied, the only 2 cases among 227 patients with angio‐oedema seen in 10 years. The absence of the inhibitor of the activated first component of complement in their serum confirmed the diagnosis. In a double blind trial their symptoms were partially controlled by ε ‐ aminocaproic acid, although there were no consistent changes in the serum complement levels. Copyright © 1969, Wiley Blackwell. All rights reserved

引用

页码：763 / &