Thrombosis associated with the prothrombin G-->A20210 mutation in Behçet's disease

J Rheumatol. 2000 Feb;27(2):515-6.

Abstract

We describe 2 cases of Behcet's disease (BD) and thrombosis who were heterozygous for the prothrombin G-->A20210 mutation. In one case, progressive uncontrolled thromboses led to death. Case-control studies are needed to support the hypothesis of the role of the prothrombin A20210 allele as a risk factor for venous thrombosis in some patients with BD.

MeSH terms

  • Adult
  • Behcet Syndrome / genetics*
  • Female
  • Humans
  • Mutation
  • Prothrombin / genetics*
  • Thrombosis / etiology*
  • Thrombosis / genetics*

Substances

  • Prothrombin