Background Hereditary angioedema (HAE), caused by deficiency in C1‐inhibitor (C1‐INH),
leads to unpredictable edema of subcutaneous tissues with potentially fatal complications …

Hereditary angioedema (HAE) is a rare autosomal dominant disease that results from
mutations in the C1-esterase inhibitor (C1-INH) gene. HAE is characterized by recurrent …

Background Hereditary angioedema is a potentially life‐threatening disorder, because
edema occurring in the mucosa of the upper airways can lead to suffocation. The …

To cite this article: Zanichelli A, Vacchini R, Badini M, Penna V, Cicardi M. Standard care
impact on angioedema because of hereditary C1 inhibitor deficiency: a 21‐month …

OBJECTIVE: To determine when newer agents, such as C1 esterase inhibitor protein (C1-
INH), should be considered as prophylaxis to decrease hereditary angioedema (HAE) …

Background Hereditary angioedema (HAE) is a disease characterized by recurrent tissue
swelling affecting various body locations. Recent literature shows that patients with frequent …

Hereditary angioedema (HAE), deficiency of C1 esterase inhibitor, poses a risk of airway
compromise during trauma, including surgery, due to activation of the complement cascade …

■ Abstract Background: Hereditary angioedema due to C1 inhibitor deficiency (HAE-C1-
INH) has considerable implications for dental health care providers, since dental procedures …

Hereditary angioedema (HAE) is a rare condition, mostly due to genetic deficiency of
complement C1 inhibitor (C1-INH). The rarity of HAE impedes extensive data collection and …

Although most hereditary angioedema (HAE) attacks appear to occur spontaneously, they
can be precipitated by emotional stressors or physical triggers, including invasive medical or …