[遗传性血管性水肿患者的家族研究]
[Familial studies of patients with hereditary angioedema].
作者信息
Bozhkov B, Nikolov K, Baleva M
出版信息
Vutr Boles. 1988;27(4):62-5.
PMID:3213025
Abstract
25 families with 607 members were studied. 165 persons of them suffer from hereditary angioneurotic edema and 28 persons had died from this disease. The clinical forms of the disease are discussed. A classification of angioneurotic edema caused by C-inactivator deficiency is presented. The importance of the examination of C1 inactivator (quantitatively and qualitatively) and of C4 complement fraction in patients with hereditary angioneurotic edema is pointed out.
摘要
对25个家庭的607名成员进行了研究。其中165人患有遗传性血管性水肿，28人死于该病。文中讨论了该病的临床症状。提出了由C1酯酶抑制剂缺乏引起的血管性水肿的分类方法。指出了对遗传性血管性水肿患者进行C1酯酶抑制剂（定量和定性）及C4补体成分检测的重要性。
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