| Literature DB >> 6899952 |
Abstract
This paper reports the findings of an "acquired" hereditary angioedema-like syndrome in a patient with myelofibrosis. No previous personal or family history of angioedema was present. The serum complement pattern showed a marked reduction of Cl esterase inhibitor, Clq and C4. All family members had a normal complement profile. Because of frequent attacks of laryngeal angioedema, prophylactic treatment with danazol was started. A striking clinical response was observed as well as a normalizing effect on the underlying biochemical abnormality.Entities:
Mesh:
Substances:
Year: 1980 PMID: 6899952
Source DB: PubMed Journal: Acta Med Scand ISSN: 0001-6101