Hereditary angioedema with C1 inhibitor deficiency (C1-INH-HAE) is characterized by recurrent swelling in subcutaneous or submucosal tissues. Symptoms often begin by age 5-11 years and worsen during puberty, but attacks can occur at any age and recur throughout life. Disease course in elderly patients is rarely reported.

Elderly versus younger patients with hereditary angioedema type I/II: patient characteristics and safety analysis from the Icatibant Outcome Survey / Bygum, Anette; Caballero, Teresa; Grumach, Anete S; Longhurst, Hilary J; Bouillet, Laurence; Aberer, Werner; Zanichelli, Andrea; Botha, Jaco; Andresen, Irmgard; Maurer, Marcus; Marone, G. - In: CLINICAL AND TRANSLATIONAL ALLERGY. - ISSN 2045-7022. - 9:1(2019), p. 37. [10.1186/s13601-019-0272-9]

Elderly versus younger patients with hereditary angioedema type I/II: patient characteristics and safety analysis from the Icatibant Outcome Survey

Marone G
2019

Abstract

Hereditary angioedema with C1 inhibitor deficiency (C1-INH-HAE) is characterized by recurrent swelling in subcutaneous or submucosal tissues. Symptoms often begin by age 5-11 years and worsen during puberty, but attacks can occur at any age and recur throughout life. Disease course in elderly patients is rarely reported.
2019
Elderly versus younger patients with hereditary angioedema type I/II: patient characteristics and safety analysis from the Icatibant Outcome Survey / Bygum, Anette; Caballero, Teresa; Grumach, Anete S; Longhurst, Hilary J; Bouillet, Laurence; Aberer, Werner; Zanichelli, Andrea; Botha, Jaco; Andresen, Irmgard; Maurer, Marcus; Marone, G. - In: CLINICAL AND TRANSLATIONAL ALLERGY. - ISSN 2045-7022. - 9:1(2019), p. 37. [10.1186/s13601-019-0272-9]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/771968
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