This study aims to review the global mortality secondary to laryngeal edema in patients
diagnosed with hereditary angioedema and their relatives over the years, as well as to …

Background This systematic study aims to assess the global epidemiologic, economic, and
humanistic burden of illness associated with all types of hereditary angioedema. Methods A …

Background Hereditary angioedema (HAE) is a rare genetic disease with significant
morbidity and mortality for which early diagnosis and effective therapy are critical. Many Asia …

Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare and life-
threatening condition characterized by recurrent localized edema. We conducted a …

Hereditary angioedema (HAE) is an uncommon disorder with a global prevalence of
approximately 1 in 10,000 to 1 in 50,000 population. This disease is grossly …

Hereditary angioedema (HAE) is a rare genetic disorder characterized by recurrent
episodes of skin and mucosal edema. The main treatment goal is to enable a “normal life” …

Hereditary angioedema (HAE) is an uncommon disorder characterized clinically by
recurrent episodes of nonitchy subcutaneous and/or submucosal swellings. The estimated …

Hereditary angioedema (HAE) is a rare genetic disorder. The pattern of HAE is different in
children as compared to adults. There is limited literature from developing countries where …

Background Hereditary angioedema (HAE) is a rare autosomal dominant disorder
characterized clinically by recurrent episodes of non-pruritic subcutaneous and/or …

Hereditary angioedema (HAE) is a potentially life-threatening autosomal dominant disorder
affecting roughly 1: 50,000 individuals. It is commonly characterized by swelling of the …