Add to ORKGWe report a 64-year-old man who suffered from recurrent visible swelling attacks since the age of 20 as well as episodes with severe upper airway edema, resulting in 4 emergency tracheotomies. Eventually after 44 years he was diagnosed with hereditary angioedema (HAE) type II. The aims of this report is to emphasize the importance of awareness concerning HAE, which does not respond to traditional anti-allergic therapy, and remind physicians to test for functional C1-INH deficiency
Background: Hereditary angioedema (HAE) is a rare but life-threatening condition that results from m...
Hereditary angioedema (HAE) is a distinctive form of recurrent angioedema with life threatening cons...
Hereditary angioedema (HAE) is a rare genetic condition whose main symptoms are recurrent swelling i...
We report a 64-year-old man who suffered from recurrent visible swelling attacks since the age of 20...
Abstract Background Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare auto...
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder which causes bradykinin me...
Hereditary angioedema (HAE) is a rare autosomal dominant disease due to C1 esterase inhibitor defici...
Background: Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare autosomal do...
Hereditary angioedema is a rare disorder characterized by a deficiency in C1 esterase inhibitor. Sym...
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 (HAE) is due to the inherited deficiency of C1-Inhibitor (C1-Inh). When specif...
Hereditary angioedema is caused by an absolute deficiency or the functional inactivity of C1 esteras...
Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) causes swelling in the skin and up...
Hereditary angioedema (HA) is caused by a quantitative or qualitative deficiency of C1 esterase inhi...
Background: Hereditary angioedema (HAE) is a rare but life-threatening condition that results from m...
Hereditary angioedema (HAE) is a distinctive form of recurrent angioedema with life threatening cons...
Hereditary angioedema (HAE) is a rare genetic condition whose main symptoms are recurrent swelling i...
We report a 64-year-old man who suffered from recurrent visible swelling attacks since the age of 20...
Abstract Background Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare auto...
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder which causes bradykinin me...
Hereditary angioedema (HAE) is a rare autosomal dominant disease due to C1 esterase inhibitor defici...
Background: Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare autosomal do...
Hereditary angioedema is a rare disorder characterized by a deficiency in C1 esterase inhibitor. Sym...
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 (HAE) is due to the inherited deficiency of C1-Inhibitor (C1-Inh). When specif...
Hereditary angioedema is caused by an absolute deficiency or the functional inactivity of C1 esteras...
Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) causes swelling in the skin and up...
Hereditary angioedema (HA) is caused by a quantitative or qualitative deficiency of C1 esterase inhi...
Background: Hereditary angioedema (HAE) is a rare but life-threatening condition that results from m...
Hereditary angioedema (HAE) is a distinctive form of recurrent angioedema with life threatening cons...
Hereditary angioedema (HAE) is a rare genetic condition whose main symptoms are recurrent swelling i...