| Literature DB >> 11990338 |
Avnish K Seth1, Velu Nair, Jasjit Singh, Ved Prakash Dhand.
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.Entities:
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Year: 2002 PMID: 11990338
Source DB: PubMed Journal: Indian J Gastroenterol ISSN: 0254-8860