Hereditary angioedema (HAE) due to a C1-esterase inhibitor(C1-INH) deficiency is a rare and potentially life-threatening disorder. It is characterized by an episodic and self-limiting increase in vascular permeability. The condition manifests itself as recurrent attacks of swelling in any part of the body. The angioedema can cause the involvement of the respiratory tract, skin, and gastrointestinal tract. Laryngeal involvement can make the condition life-threatening. It does not respond well to conventional angioedema therapy of steroids, adrenaline, and antihistamines. The targeted therapy for HAE consists of plasma-derived or recombinant C1-INH, ecallantide, and icatibant or bradykinin receptor antagonist. In the absence of these therapie...
type I in a female patient: a case report Hereditary angioedema (HAE) is rare autosomal dominant dis...
Background: Hereditary angioedema is a disease which manifests itself with episodes of spontaneous e...
Hereditary angioedema (HAE) is arare, potentially life-threatening au-tosomal dominant disease cause...
Hereditary angioedema (HAE) due to a C1-esterase inhibitor(C1-INH) deficiency is a rare and potentia...
Hereditary angioedema (HAE) is a rarely seen disorder of C1 inhibitor (C1-INH) deficiency usually ma...
WOS: 000248892300008PubMed ID: 17692764Hereditary angioedema (HAE) is a rarely seen disorder of C1 i...
Objectives: Fresh frozen plasma (FFP) has been used in angioedema crises, however there is a risk of...
Abstract Hereditary angioedema (HAE) is a rare autosomal dominant disease most commonl...
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...
Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a rare genetic disease charac...
Abstract Hereditary angioedema (HAE) is a rare, mostly inherited disorder however 25% of patients...
Hereditary angioedema (HAE) is an autosomal dominantly inherited orphan disease manifested by recurr...
C1-inhibitor (C1-INH) deficiency is the genetic defect underlying hereditary angioedema (HAE). Subje...
Patients with angioedema who experience an acute exacerbation may die if their symptoms are not trea...
Hereditary angioedema (HAE), a rare autosomal dominant genetic disorder, is caused by a deficiency i...
type I in a female patient: a case report Hereditary angioedema (HAE) is rare autosomal dominant dis...
Background: Hereditary angioedema is a disease which manifests itself with episodes of spontaneous e...
Hereditary angioedema (HAE) is arare, potentially life-threatening au-tosomal dominant disease cause...
Hereditary angioedema (HAE) due to a C1-esterase inhibitor(C1-INH) deficiency is a rare and potentia...
Hereditary angioedema (HAE) is a rarely seen disorder of C1 inhibitor (C1-INH) deficiency usually ma...
WOS: 000248892300008PubMed ID: 17692764Hereditary angioedema (HAE) is a rarely seen disorder of C1 i...
Objectives: Fresh frozen plasma (FFP) has been used in angioedema crises, however there is a risk of...
Abstract Hereditary angioedema (HAE) is a rare autosomal dominant disease most commonl...
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...
Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a rare genetic disease charac...
Abstract Hereditary angioedema (HAE) is a rare, mostly inherited disorder however 25% of patients...
Hereditary angioedema (HAE) is an autosomal dominantly inherited orphan disease manifested by recurr...
C1-inhibitor (C1-INH) deficiency is the genetic defect underlying hereditary angioedema (HAE). Subje...
Patients with angioedema who experience an acute exacerbation may die if their symptoms are not trea...
Hereditary angioedema (HAE), a rare autosomal dominant genetic disorder, is caused by a deficiency i...
type I in a female patient: a case report Hereditary angioedema (HAE) is rare autosomal dominant dis...
Background: Hereditary angioedema is a disease which manifests itself with episodes of spontaneous e...
Hereditary angioedema (HAE) is arare, potentially life-threatening au-tosomal dominant disease cause...