Four patients with hereditary angioedema with different initial symptoms and clinical features.
作者信息
Chen Jiao, Wang Ruiyu, Zhang Shun, Wang Yang, Chen Ying, Zhang Xiaohong, Lyu Chuanzhu
机构信息
1Department of Emergency Medicine Center, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan 610072, China.
2Emergency Department, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100730, China.
出版信息
World J Emerg Med. 2025 May 1;16(3):283-285. doi: 10.5847/wjem.j.1920-8642.2025.060.
Abstract
摘要
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Hereditary Angioedema: Diagnosis, Clinical Implications, and Pathophysiology.遗传性血管性水肿：诊断、临床意义和病理生理学。
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Treatment of Hereditary Angioedema.遗传性血管性水肿的治疗。
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Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N-terminal cleavage site of bradykinin.遗传性血管性水肿与一种新型激肽原1基因突变共分离，该突变改变了缓激肽的N端切割位点。
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Hereditary angioedema with a mutation in the plasminogen gene.遗传性血管性水肿伴纤溶酶原基因突变。
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Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema.血管生成素-1 基因（ANGPT1）的突变与一种新型遗传性血管性水肿有关。
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Hereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe.遗传性血管性水肿伴 C1 抑制剂缺乏症：在欧洲的诊断延迟。
Allergy Asthma Clin Immunol. 2013 Aug 12;9(1):29. doi: 10.1186/1710-1492-9-29.
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