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Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder related to low levels of C1 inhibitor, which lead to too much of the plasma kallikrein enzyme, triggering overproduction of ...

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Its not always possible to know when a hereditary angioedema (HAE) attack will strike. But specific triggers account for about 40 percent of attacks, causing painful swelling throughout the body.

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Hereditary angioedema (HAE) is diagnosed through blood tests that measure complement protein (C4) and complement inhibitor (C1-INH) levels. Low C4 levels strongly suggest HAE, especially during an ...

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Hereditary angioedema is a rare disorder that leads to repeated episodes of severe swelling, most often in the face, limbs, intestinal tract, and airway. Symptoms vary depending on where these ...