Add to ORKGHereditary angioedema (HA) is caused by a quantitative or qualitative deficiency of C1 esterase inhibitor (C1 INH). We present a study of nine patients with HA belonging to two different families. The symptoms started before 10 years of age in most cases (78%). Facial edema (lips, eyes) and of the extremities (feet, hands) were the most frequent complaints. Three patients presented edema of the glottis and one of them underwent a tracheostomy twice. Laboratory tests, outside the acute crisis, revealed low levels of C4 in all patients. The serum levels of C1 INH were normal in seven patients; however, functional activity was not observed in any of them. After the use of a modified androgen (danazol), control of symptoms was observed in all p...
Background: Hereditary angioedema (HAE) is a rare autosomal dominant disorder characterized by C1-IN...
Hereditary angioedema secondary to C1-inhibitor deficiency is a rare autosomal dominant disorder cha...
Diagnosis and treatment of hereditary angioneurotic oedema (HAO) is described in a family. C1 estera...
One hundred and four patients affected by hereditary angioedema belonging to 31 families have been s...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE) is a rare autosomal dominant disease due to C1 esterase inhibitor defici...
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...
Two hundred and twenty-six patients with inherited C1 inhibitor (C1-INH) deficiency, also known as h...
Hereditary angioedema (HAE) is a distinctive form of recurrent angioedema with life threatening cons...
A new type of hereditary angioedema was described recently. It was characterized by recurrent bouts ...
Hereditary angioedema (HAE) with normal C1-inhibitor level is a rare potentially life-threatening di...
Hereditary angioedema is caused by an absolute deficiency or the functional inactivity of C1 esteras...
Hereditary angioedema (HAE) caused by a deficiency of C1 esterase inhibitor enzyme (C1-INH) is a ver...
Background: Hereditary angioedema (HAE) is a rare autosomal dominant disorder characterized by C1-IN...
Hereditary angioedema secondary to C1-inhibitor deficiency is a rare autosomal dominant disorder cha...
Diagnosis and treatment of hereditary angioneurotic oedema (HAO) is described in a family. C1 estera...
One hundred and four patients affected by hereditary angioedema belonging to 31 families have been s...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE) is a rare autosomal dominant disease due to C1 esterase inhibitor defici...
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...
Two hundred and twenty-six patients with inherited C1 inhibitor (C1-INH) deficiency, also known as h...
Hereditary angioedema (HAE) is a distinctive form of recurrent angioedema with life threatening cons...
A new type of hereditary angioedema was described recently. It was characterized by recurrent bouts ...
Hereditary angioedema (HAE) with normal C1-inhibitor level is a rare potentially life-threatening di...
Hereditary angioedema is caused by an absolute deficiency or the functional inactivity of C1 esteras...
Hereditary angioedema (HAE) caused by a deficiency of C1 esterase inhibitor enzyme (C1-INH) is a ver...
Background: Hereditary angioedema (HAE) is a rare autosomal dominant disorder characterized by C1-IN...
Hereditary angioedema secondary to C1-inhibitor deficiency is a rare autosomal dominant disorder cha...
Diagnosis and treatment of hereditary angioneurotic oedema (HAO) is described in a family. C1 estera...