Factor II gene(prothrombin G20210A)mutation and neonatal cerebrovenous thrombosis

Thromb Haemost. 2004 Oct;92(4):719-21.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Cerebral Hemorrhage
  • DNA Mutational Analysis
  • Family Health
  • Female
  • Humans
  • Infant, Newborn
  • Intracranial Thrombosis / diagnosis
  • Intracranial Thrombosis / etiology*
  • Intracranial Thrombosis / genetics
  • Male
  • Point Mutation*
  • Prothrombin / genetics*
  • Risk Factors
  • Venous Thrombosis / diagnosis
  • Venous Thrombosis / etiology*
  • Venous Thrombosis / genetics

Substances

  • Prothrombin