Hereditary angioedema (HAE) is an autosomal-dominant disorder resulting from C1-inhibitor (C1INH) deficiency. Smell impairments were found in patients affected with systemic lupus erythematosus, that, similarly to HAE, is characterized by the activation of the classical complement pathway with C4 consumption. In this study, we aimed at evaluating the sense of smell in patients with HAE.

Perricone, C., Agmon Levin, N., Shoenfeld, N., de Carolis, C., Guarino, M.d., Gigliucci, G., et al. (2011). Evidence of impaired sense of smell in hereditary angioedema. ALLERGY, 66(1), 149-154 [10.1111/j.1398-9995.2010.02453.x].

Evidence of impaired sense of smell in hereditary angioedema

GUARINO, MARIA DOMENICA;PERRICONE, ROBERTO;
2011-01-01

Abstract

Hereditary angioedema (HAE) is an autosomal-dominant disorder resulting from C1-inhibitor (C1INH) deficiency. Smell impairments were found in patients affected with systemic lupus erythematosus, that, similarly to HAE, is characterized by the activation of the classical complement pathway with C4 consumption. In this study, we aimed at evaluating the sense of smell in patients with HAE.
gen-2011
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
English
Humans; Smell; Complement C4; Complement Hemolytic Activity Assay; Olfaction Disorders; Angioedemas, Hereditary; Lupus Erythematosus, Systemic; Complement Pathway, Classical; Adult; Case-Control Studies; Middle Aged; Complement C1 Inhibitor Protein; Female; Male
Perricone, C., Agmon Levin, N., Shoenfeld, N., de Carolis, C., Guarino, M.d., Gigliucci, G., et al. (2011). Evidence of impaired sense of smell in hereditary angioedema. ALLERGY, 66(1), 149-154 [10.1111/j.1398-9995.2010.02453.x].
Perricone, C; Agmon Levin, N; Shoenfeld, N; de Carolis, C; Guarino, Md; Gigliucci, G; Milana, I; Novelli, L; Valesini, G; Perricone, R; Shoenfeld, Y
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/51696
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