Results: 2

Hereditary angioedema with C1 inhibitor (C1-INH) deficit: the strength of recognition (51 cases)

Fragnan, N T M L; Tolentino, A L N; Borba, G B; Oliveira, A C; Simões, J A; Palma, SM U; Constantino-Silva, R N; Grumach, A S.

Braz. j. med. biol. res; 51 (12), 2018

Hereditary angioedema (HAE) is a rare autosomal dominant disease due to C1 esterase inhibitor deficiency (C1-INH). The disease is characterized by subcutaneous and submucosal edema in the absence of urticaria due to the accumulation of bradykinin. This descriptive study aimed to evaluate the clinical cha...

Edad de Inicio, Antifibrinolíticos/uso terapéutico, Proteína Inhibidora del Complemento C1/análisis, Antagonistas de Estrógenos/uso terapéutico, Angioedema Hereditario Tipos I y II/sangre, Angioedema Hereditario Tipos I y II/tratamiento farmacológico, Angioedema Hereditario Tipos I y II/etiología, Angioedema Hereditario Tipos I y II/prevención & control, Hospitalización, Nefelometría y Turbidimetría/métodos, Profilaxis Posexposición/métodos, Factores Desencadenantes, Trauma Psicológico/complicaciones, Factores de Riesgo, Estrés Psicológico/complicaciones, Resultado del Tratamiento

Fulltext

Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis

Clinics; 73 (), 2018

Hereditary angioedema is an autosomal dominant disease characterized by recurrent angioedema attacks with the involvement of multiple organs. The disease is unknown to many health professionals and is therefore underdiagnosed. Patients who are not adequately diagnosed and treated have an estimated mortal...

Angioedemas Hereditarios/clasificación, Angioedemas Hereditarios/diagnóstico, Angioedemas Hereditarios/fisiopatología, Brasil, Proteína Inhibidora del Complemento C1/análisis, Complemento C4/análisis, Diagnóstico Diferencial

Fulltext