A novel nonsense mutation in the antithrombin III gene (Cys-4-->stop) causing recurrent venous thrombosis

Blood Coagul Fibrinolysis. 1996 Jul;7(5):578-9. doi: 10.1097/00001721-199607000-00010.

Abstract

We describe a novel mutation identified in the antithrombin III (AT-III) propeptide responsible for AT-III deficiency. This mutation, a C to A transversion in exon 2, converts the cysteine at position -4 into a stop codon (TGC-->TGA). In this family with severe thrombophilia, the mutation co-segregates with the clinical phenotype.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antithrombin III / genetics*
  • Antithrombin III Deficiency
  • Disease Susceptibility
  • Exons / genetics
  • Female
  • Humans
  • Intracranial Embolism and Thrombosis / blood
  • Intracranial Embolism and Thrombosis / etiology*
  • Male
  • Pedigree
  • Point Mutation*
  • Polymerase Chain Reaction
  • Recurrence
  • Thrombophlebitis / blood
  • Thrombophlebitis / etiology*

Substances

  • Antithrombin III