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Article in English | IMSEAR | ID: sea-64156

ABSTRACT

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.


Subject(s)
Abdominal Pain/etiology , Adult , Angioedema/genetics , Complement C1 Inactivator Proteins/deficiency , Danazol/therapeutic use , Humans , Male
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