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Hereditary angioedema ( HAE) is a disorder that results in recurrent attacks of severe swelling. [3] The swelling most commonly affects the arms, legs, face, intestinal tract, and airway. [3] If the intestinal tract is affected, abdominal pain and vomiting may occur. [1]
May 1, 2023 · Hereditary angioedema (HAE) is an autosomal dominant disease caused by the lack of or a dysfunctional C1-inhibitor protein. For this reason, the nomenclature has been developed to replace the initial use of type 1, 2, or 3 HAE.
Hereditary angioedema is a rare genetic condition that causes swelling under the skin and lining of the gut and lungs. Learn about the symptoms, triggers, diagnosis, and treatment options for this disease that can be life-threatening.
Hereditary angioedema (HAE) is a rare genetic condition that causes severe swelling in various body parts. Learn about the types, triggers, diagnosis, and treatment options for this condition that can be life threatening.
Hereditary angioedema (HAE) is a disease characterized by recurrent episodes (also called attacks) of severe swelling of the skin and mucous membranes. The frequency of attacks usually increases after puberty.
Hereditary angioedema is a rare genetic disorder that causes recurrent episodes of oedema in the skin, gastrointestinal tract, and airways. Learn about the different types of hereditary angioedema, how they are diagnosed, and what treatments are available.
Learn about the causes, symptoms, and types of hereditary angioedema, a disorder that causes severe swelling in various parts of the body. Find out how this condition is inherited and what treatments are available.
