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Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition Classification and Diagnosis

机译:巴西遗传性血管性水肿管理指南-2017年更新第1部分:定义分类和诊断

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摘要

Hereditary angioedema is an autosomal dominant disease characterized by recurrent angioedema attacks with the involvement of multiple organs. The disease is unknown to many health professionals and is therefore underdiagnosed. Patients who are not adequately diagnosed and treated have an estimated mortality rate ranging from 25% to 40% due to asphyxiation by laryngeal angioedema. Intestinal angioedema is another important and incapacitating presentation that may be the main or only manifestation during an attack. In this article, a group of experts from the “Associação Brasileira de Alergia e Imunologia (ASBAI)” and the “Grupo de Estudos Brasileiro em Angioedema Hereditário (GEBRAEH)” has updated the Brazilian guidelines for the diagnosis and treatment of hereditary angioedema.
机译:遗传性血管性水肿是一种常染色体显性疾病,其特征是反复发作的血管性水肿伴有多个器官。该疾病是许多卫生专业人员未知的,因此未得到充分诊断。由于喉部血管性水肿窒息,未得到充分诊断和治疗的患者估计死亡率为25%至40%。肠血管性水肿是另一个重要且无功能的表现,可能是发作期间的主要或唯一表现。在本文中,来自“巴西利亚免疫性疾病协会(ASBAI)”和“巴西埃斯托多斯遗传性血管性水疱病(GEBRAEH)”的专家组对巴西诊断和治疗遗传性血管性水肿的指南进行了更新。

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