The importance of recognizing and managing a rare form of angioedema: hereditary angioedema due to C1-inhibitor deficiency
Author:
Affiliation:
1. Allergy and Asthma Clinical Research, Inc. Walnut Creek, CA
2. Dept of Internal Medicine, Northern CA VA Health Care System, Martinez Outpatient Clinic
Funder
provided by CSL Behring
Publisher
Informa UK Limited
Subject
General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/00325481.2021.1905364
Reference125 articles.
1. 1. Maurer M, Magerl M, Ansotegui I, et al. The international WAO/EAACI guideline for the management of hereditary angioedema-The 2017 revision and update. Allergy. 2018;73(8):1575–1596.
2. 2. Cicardi M, Bergamaschini B, Marasini B, et al. Hereditary angioedema: an appraisal of 104 cases. Am J Med Sci. 1982;284(1):2–9.
3. 3. Bork K, Meng G, Staubach P, et al. Hereditary angioedema: new findings concerning symptoms, affected organs, and course. Am J Med. 2006;119:267–274.
4. 4. Lumry W, Templeton T, Omert L, et al. Advances in hereditary angioedema: the prevention of angioedema attacks with subcutaneous C1-inhibitor replacement therapy. J Infus Nurs, 2020;43(3):134–145.
5. 5. Bernstein JA, Cremonesi P, Hoffmann TK, et al. Angioedema in the emergency department: a practical guide to differential diagnosis and management. Int J Emerg Med. 2017;10(1):15.
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