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.File in questo prodotto:
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