Matter L, Schopfer K, Voegelin H P, Fueter R
Schweiz Med Wochenschr. 1981 Aug 22;111(34):1238-45.
Report on a newly recognized sibship with hereditary angioedema (HAE). The 27 persons investigated include 8 with decreased concentrations of C-1INH and C4 in the Serum. Three of these are children without symptoms of HAE. Five patients have characteristic attacks of HAE, some of which are predominantly abdominal. The effects of treatment with danazol in 4 patients are described. HAE is briefly reviewed with special reference to pathogenesis and treatment.
关于一个新确认的遗传性血管性水肿(HAE)家族的报告。接受调查的27人中有8人血清中C-1INH和C4浓度降低。其中3名是没有HAE症状的儿童。5名患者有HAE的典型发作,有些主要是腹部发作。描述了4名患者使用达那唑治疗的效果。对HAE进行了简要综述,特别提及了发病机制和治疗方法。