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- W2762898034 abstract "Hereditary angioedema (HAE) is a rare, autosomal dominant condition that consists of a deficiency or dysfunction of C1 esterase inhibitor (C1-INH). Various triggers can lead to self-limiting or life-threatening airway edema. [1] Zuraw B.L. Bork K. Binkley K.E. et al. Hereditary angioedema with normal C1 inhibitor function: consensus of an international expert panel. Allergy Asthma Proc. 2012; 33: S145-S156 Crossref PubMed Scopus (145) Google Scholar Owing to its nonhistaminergic pathophysiologic features, HAE subtypes do not respond to epinephrine, corticosteroids, or antihistamine. Supplementation of C1-INH is an accepted and common treatment for HAE attacks and HAE prophylaxis." @default.
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- W2762898034 date "2017-12-01" @default.
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- W2762898034 title "Successful perinatal management of hereditary angioedema with normal C1 esterase inhibitor and factor XII mutation using C1 esterase inhibitor therapy" @default.
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- W2762898034 doi "https://doi.org/10.1016/j.anai.2017.08.015" @default.
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