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Four patients with hereditary angioedema with different initial symptoms and clinical features.四名患有遗传性血管性水肿的患者，具有不同的初始症状和临床特征。
World J Emerg Med. 2025 May 1;16(3):283-285. doi: 10.5847/wjem.j.1920-8642.2025.060.
2
Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course.C1抑制物正常的遗传性血管性水肿：临床症状与病程
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Clinical Evaluation of Pediatric Patients with Hereditary Angioedema.遗传性血管性水肿患儿的临床评估。
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Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence.遗传性血管性水肿伴正常 C1 抑制剂的基因特征类型的临床特征：定性证据的系统评价。
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[Diagnosis and treatment of hereditary angioedema with normal C1-inhibitor level].C1抑制物水平正常的遗传性血管性水肿的诊断与治疗
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Idiopathic Nonhistaminergic Acquired Angioedema Versus Hereditary Angioedema.特发性非组胺性获得性血管性水肿与遗传性血管性水肿。
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本文引用的文献

1
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。
Adv Ther. 2023 Mar;40(3):814-827. doi: 10.1007/s12325-022-02401-0. Epub 2023 Jan 7.
2
Treatment of Hereditary Angioedema.遗传性血管性水肿的治疗。
J Investig Allergol Clin Immunol. 2021 Feb;31(1):1-16. doi: 10.18176/jiaci.0653.
3
Clinical presentation of hereditary angioedema.遗传性血管性水肿的临床表现。
Allergy Asthma Proc. 2020 Nov 1;41(Suppl 1):S18-S21. doi: 10.2500/aap.2020.41.200065.
4
Hereditary Angioedema.遗传性血管性水肿
N Engl J Med. 2020 Mar 19;382(12):1136-1148. doi: 10.1056/NEJMra1808012.
5
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。
Allergy. 2019 Dec;74(12):2479-2481. doi: 10.1111/all.13869. Epub 2019 Jun 7.
6
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。
Allergy. 2018 Feb;73(2):442-450. doi: 10.1111/all.13270. Epub 2017 Sep 7.
7
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。
J Allergy Clin Immunol. 2018 Mar;141(3):1009-1017. doi: 10.1016/j.jaci.2017.05.020. Epub 2017 Jun 8.
8
Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations.遗传性血管性水肿伴正常 C1-INH 与有无特定 F12 基因突变。
Allergy. 2015 Aug;70(8):1004-12. doi: 10.1111/all.12648. Epub 2015 May 22.
9
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.

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.

DOI:10.5847/wjem.j.1920-8642.2025.060
PMID:40406293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12093428/
Abstract
摘要