Hereditary angio-oedema is characterised by recurrent swellings in any part of the body and also by recurrent attacks of severe abdominal pain. The disease is inherited in an autosomal dominant manner but up to 25 % of cases can occur as a spontaneous mutation. Attacks of swelling can be precipitated by trauma, certain drugs, and emotional stress. Treatment usually involves a combination of prophylaxis, using androgens or antifibrolytic drugs, and replacement with C’1 esterase inhibitor concentrate for acute attacks and before surgery or other traumatic procedures. Hereditary angio-oedema (HAE) is charac-terised by recurrence of cutaneous andmucous membrane swellings in any part of the body. Symptoms usually appear early in life and are nor...
Hereditary angioedema (HAE) is a rare genetic condition that manifests as painful and potentially li...
Hereditary angioedema is a rare, genetic disorder characterized by painful, debilitating and potenti...
Hereditary angioedema is a rare autosomal dominant disorder caused by reduced activity of the C1 est...
SummaryHereditary angio-oedema is caused by a heterozygous deficiency of C1 inhibitor. This inhibito...
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) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE) is a rare autosomal-dominant disorder; most cases are characterized by l...
Hereditary angioedema (HAE) caused by a deficiency of C1 esterase inhibitor enzyme (C1-INH) is a ver...
Abstract: Hereditary angioedema (HAE) caused by C1-esterase inhib-itor deficiency is an autosomal-do...
One hundred and four patients affected by hereditary angioedema belonging to 31 families have been s...
Hereditary angioedema is a rare autosomal dominant disease characterized by recurrent episodes of an...
Hereditary angioedema is a rare autosomal dominant disorder resulting from the congenital deficiency...
Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a rare genetic disease charac...
Hereditary angioedema (HAE) is a rare genetic condition that manifests as painful and potentially li...
Hereditary angioedema is a rare, genetic disorder characterized by painful, debilitating and potenti...
Hereditary angioedema is a rare autosomal dominant disorder caused by reduced activity of the C1 est...
SummaryHereditary angio-oedema is caused by a heterozygous deficiency of C1 inhibitor. This inhibito...
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) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE) is a rare autosomal-dominant disorder; most cases are characterized by l...
Hereditary angioedema (HAE) caused by a deficiency of C1 esterase inhibitor enzyme (C1-INH) is a ver...
Abstract: Hereditary angioedema (HAE) caused by C1-esterase inhib-itor deficiency is an autosomal-do...
One hundred and four patients affected by hereditary angioedema belonging to 31 families have been s...
Hereditary angioedema is a rare autosomal dominant disease characterized by recurrent episodes of an...
Hereditary angioedema is a rare autosomal dominant disorder resulting from the congenital deficiency...
Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a rare genetic disease charac...
Hereditary angioedema (HAE) is a rare genetic condition that manifests as painful and potentially li...
Hereditary angioedema is a rare, genetic disorder characterized by painful, debilitating and potenti...
Hereditary angioedema is a rare autosomal dominant disorder caused by reduced activity of the C1 est...