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Artigo em Inglês | IMSEAR | ID: sea-64156

RESUMO

Hereditary angioedema is a rare disorder characterized by quantitative or qualitative deficiency of complement C1 esterase inhibitor. We report a family whose members presented with recurrent angioedema and abdominal pain; the diagnosis was confirmed by quantitative assay of C1 inhibitor. The index patient was treated with danazol and was relieved.


Assuntos
Dor Abdominal/etiologia , Adulto , Angioedema/genética , Proteínas Inativadoras do Complemento 1/deficiência , Danazol/uso terapêutico , Humanos , Masculino
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