Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) causes swelling in the skin and upper airways and pain in the abdomen because of mucosal swelling. C1-INH-HAE is frequently misdiagnosed, leading to delays in diagnosis, inadequate treatment, and unnecessary procedures.

Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting / Zanichelli, Andrea; Longhurst, Hilary J; Maurer, Marcus; Bouillet, Laurence; Aberer, Werner; Fabien, Vincent; Andresen, Irmgard; Caballero, Teresa; Marone, Gianni. - In: ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY. - ISSN 1081-1206. - 117:4(2016), pp. 394-398. [10.1016/j.anai.2016.08.014]

Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting

MARONE, GIANNI
2016

Abstract

Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) causes swelling in the skin and upper airways and pain in the abdomen because of mucosal swelling. C1-INH-HAE is frequently misdiagnosed, leading to delays in diagnosis, inadequate treatment, and unnecessary procedures.
2016
Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting / Zanichelli, Andrea; Longhurst, Hilary J; Maurer, Marcus; Bouillet, Laurence; Aberer, Werner; Fabien, Vincent; Andresen, Irmgard; Caballero, Teresa; Marone, Gianni. - In: ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY. - ISSN 1081-1206. - 117:4(2016), pp. 394-398. [10.1016/j.anai.2016.08.014]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/666891
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