面向初级保健医生的遗传性血管性水肿概述。

IF 3.8 2区医学 Q1 MEDICINE, GENERAL & INTERNAL

Medical Clinics of North America Pub Date : 2024-05-28 DOI:10.1016/j.mcna.2023.08.005

Arindam Sarkar MD , Crystal Nwagwu MD , Timothy Craig DO

引用次数: 0

摘要

遗传性血管性水肿是一种罕见的常染色体显性遗传病，其特征是上呼吸道、肠道和皮肤发生肿胀。这种疾病的特征是缺乏 C1 酯酶抑制剂（C1-INH）或功能性 C1-INH 减少。治疗方法包括按需治疗（治疗急性发作）、长期预防和短期预防。皮质类固醇、肾上腺素和抗组胺药对这种形式的血管性水肿无效。未确诊患者的死亡率很高，这凸显了医生需要更广泛地认识这些患者并开始治疗。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Medical Clinics of North America 医学-医学：内科

CiteScore

10.20

自引率

1.70%

发文量

140

审稿时长

6-12 weeks

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