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Hereditary Angioedema- A Rare Case Report and Literature Review

Hereditary angioedema (HAE) is a rare disorder due to either deficiency or dysfunction of Complement 1 (C1) esterase inhibitor (C1-INH). HAE usually presents with recurrent angioedema (AE) episodes affecting the extremities, face, and gastrointestinal tract, but it is not associated with urticarial...

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Autori principali: Charan Neeradi, Vishakha Jain, Janaradhan P. Reddy, Sugunakar Reddy, Ilakkiya Priya
Natura: Artigo
Lingua:Inglês
Pubblicazione: Wolters Kluwer Medknow Publications 2024-01-01
Serie:Annals of Rheumatology and Autoimmunity
Soggetti:
bradykinin-mediated angioedema
c1 inhibitor
guidelines
hereditary angioedema
management
Accesso online:https://journals.lww.com/10.4103/ara.ara_4_24
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