Hereditary angioedema is an autosomal dominant genetic disorder due to the deficiency of CI esterase inhibitor with elevated levels of bradykinin. The disorder was named hereditary angioneurotic edema because of the associated mental stress which exacerbated the condition. It manifests most often as edema of the skin and mucosal surfaces. Laryngeal edema can cause fatal obstruction. The various treatment modalities available for HAE includes plasma derived C1-INH concentrate, ecallantide, icatibant, attenuated androgens and fresh frozen plasma. The drugs for HAE are efficacious, but with side effects and are expensive. Patients with HAE exhibit anxiety and depression, and the stressful state by itself predisposes to further attacks which in...
Abstract Objective This study systematically reviews the existing literature on the management of he...
Hereditary angioedema (HAE) is a chronic disease with a high burden of disease that is poorly unders...
Hereditary angioedema is a rare, genetic disorder characterized by painful, debilitating and potenti...
Chronic conditions, whether genetic or acquired, impose a significant burden on health care systems ...
Hereditary angioedema (HAE) is a rare disease that causes episodic attacks of subcutaneous and submu...
This symposium provided an overview of past, current, and future therapies and routes of administrat...
Abstract Hereditary angioedema (HAE) is a rare, mostly inherited disorder however 25% of patients...
Hereditary angioedema (HAE) is a rare genetic condition that manifests as painful and potentially li...
Hereditary angioedema (HAE) is a rare autosomal-dominant disorder; most cases are characterized by l...
Hereditary angioedema (C1 inhibitor deficiency, HAE) is associated with intermittent swellings which...
Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a rare genetic disease charac...
Hereditary angioedema (HAE) is an autosomal dominantly inherited orphan disease manifested by recurr...
Hereditary Angioedema (HAE) is considered an autosomal dominant disorder, characterized by a quantit...
Abstract Current strategies for the treatment of hereditary angioedema (HAE) include targeted inhibi...
Hereditary angioedema (HAE) is arare, potentially life-threatening au-tosomal dominant disease cause...
Abstract Objective This study systematically reviews the existing literature on the management of he...
Hereditary angioedema (HAE) is a chronic disease with a high burden of disease that is poorly unders...
Hereditary angioedema is a rare, genetic disorder characterized by painful, debilitating and potenti...
Chronic conditions, whether genetic or acquired, impose a significant burden on health care systems ...
Hereditary angioedema (HAE) is a rare disease that causes episodic attacks of subcutaneous and submu...
This symposium provided an overview of past, current, and future therapies and routes of administrat...
Abstract Hereditary angioedema (HAE) is a rare, mostly inherited disorder however 25% of patients...
Hereditary angioedema (HAE) is a rare genetic condition that manifests as painful and potentially li...
Hereditary angioedema (HAE) is a rare autosomal-dominant disorder; most cases are characterized by l...
Hereditary angioedema (C1 inhibitor deficiency, HAE) is associated with intermittent swellings which...
Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a rare genetic disease charac...
Hereditary angioedema (HAE) is an autosomal dominantly inherited orphan disease manifested by recurr...
Hereditary Angioedema (HAE) is considered an autosomal dominant disorder, characterized by a quantit...
Abstract Current strategies for the treatment of hereditary angioedema (HAE) include targeted inhibi...
Hereditary angioedema (HAE) is arare, potentially life-threatening au-tosomal dominant disease cause...
Abstract Objective This study systematically reviews the existing literature on the management of he...
Hereditary angioedema (HAE) is a chronic disease with a high burden of disease that is poorly unders...
Hereditary angioedema is a rare, genetic disorder characterized by painful, debilitating and potenti...