Hereditary Angioedema: A Review

WMJ. 2022 Apr;121(1):48-53.

Abstract

Hereditary angioedema (HAE) is a rare and disabling disorder wherein there is excessive bradykinin production, with subsequent increased vascular permeability in the superficial tissues and gastrointestinal and respiratory mucosa. This article serves as a review of the pathogenesis of the disease, as well as an update of the evidence-based new treatment recommendations to help clinicians with the diagnosis and management of HAE.

Publication types

  • Review

MeSH terms

  • Angioedemas, Hereditary* / diagnosis
  • Angioedemas, Hereditary* / therapy
  • Blindness
  • Bradykinin / therapeutic use
  • Complement C1 Inhibitor Protein
  • Humans

Substances

  • Complement C1 Inhibitor Protein
  • Bradykinin