Hereditary angioedema (HAE) is a rare condition, first described by Quincke in 1882. Diminished levels of the C1 inhibitor protein of dysfunctional forms of the same protein are basis of this disease pathophysiology. We mark out three types of HAE. Type I, most common, is related with C1 INH insufficiency, type II – with its abnormal function. Mucous oedemas are characteristic for these diseases, including face and larynx oedema. Oedema involving larynx can be life‑threatening condition. HAE swelling can be caused by some drugs, especially from angiotensin convertase inhibitors group, stress, trauma, infections. Surgical procedures can predispose to HAE related larynx swelling. Surgery preparation can involve continuous intubation tube cuff...
Hereditary angioedema (HA) is caused by a quantitative or qualitative deficiency of C1 esterase inhi...
Hereditary angioedema (HAE) is a rare genetic disorder causing a deficiency in C1 esterase inhibitor...
Hereditary angioedema (HAE) is a rare autosomal dominant disease that results from mutations in the ...
Hereditary angioedema (HAE) is a rare autosomal dominant disorder caused by reduced activity of the ...
Hereditary Angioedema (HAE) is a rare disease characterized by a deficiency or a reduced function of...
Hereditary angioedema (HAE) is an autosomal dominantly inherited orphan disease manifested by recurr...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Abstract Hereditary angioedema (HAE) is a rare, mostly inherited disorder however 25% of patients...
Hereditary angioedema is a rare autosomal dominant disorder caused by reduced activity of the C1 est...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE) is a rare condition affecting about 1 in 50.000 individuals and caused b...
Hereditary angioedema (HAE) is rare autosomal dominant disease, characterised by spontaneous and rec...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE) is a rare genetic disease caused by an autosomal dominant mutation that ...
Recognition of the unique clinical and immunological characteristics of the rare causes of Hereditar...
Hereditary angioedema (HA) is caused by a quantitative or qualitative deficiency of C1 esterase inhi...
Hereditary angioedema (HAE) is a rare genetic disorder causing a deficiency in C1 esterase inhibitor...
Hereditary angioedema (HAE) is a rare autosomal dominant disease that results from mutations in the ...
Hereditary angioedema (HAE) is a rare autosomal dominant disorder caused by reduced activity of the ...
Hereditary Angioedema (HAE) is a rare disease characterized by a deficiency or a reduced function of...
Hereditary angioedema (HAE) is an autosomal dominantly inherited orphan disease manifested by recurr...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Abstract Hereditary angioedema (HAE) is a rare, mostly inherited disorder however 25% of patients...
Hereditary angioedema is a rare autosomal dominant disorder caused by reduced activity of the C1 est...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE) is a rare condition affecting about 1 in 50.000 individuals and caused b...
Hereditary angioedema (HAE) is rare autosomal dominant disease, characterised by spontaneous and rec...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE) is a rare genetic disease caused by an autosomal dominant mutation that ...
Recognition of the unique clinical and immunological characteristics of the rare causes of Hereditar...
Hereditary angioedema (HA) is caused by a quantitative or qualitative deficiency of C1 esterase inhi...
Hereditary angioedema (HAE) is a rare genetic disorder causing a deficiency in C1 esterase inhibitor...
Hereditary angioedema (HAE) is a rare autosomal dominant disease that results from mutations in the ...