Category: Immunology / Complement Disorder
Hereditary Angioedema (HAE) is a rare genetic disorder characterized by recurrent episodes of severe swelling (angioedema) in various body parts, including the skin, gastrointestinal tract, and upper airways, due to a deficiency or dysfunction of C1-esterase inhibitor.
Estimated 1 in 50,000 to 1 in 100,000 people globally. (Source: HAE Association)
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