First Reported Case of Hereditary Angioedema Due to MYOF Gene Mutation in Saudi Arabia

World Allergy Organization Journal 2026 Open access

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Authors: Afnan Ayed O Almutairi, Rand K. Arnaout
DOI: 10.1016/j.waojou.2026.101288
Cited by: 0

Abstract

Hereditary angioedema (HAE) is a rare autosomal dominant disorder, affecting approximately 1 in 50,000 individuals. It is characterized by recurrent episodes of angioedema involving the skin, upper airway, and/or gastrointestinal tract, due to increased bradykinin-mediated vascular permeability.

Fields of Study & Subjects

Coagulation Bradykinin Polyphosphates and Angioedema Connective tissue disorders research Complement system in diseases

Publication details

Journal / source
World Allergy Organization Journal
Volume
19
Issue
2
Pages
101288–101288
Publication date
1 February 2026
Language
EN