Prothrombin G20210A gene variant is not associated with idiopathic portal vein thrombosis in an area endemic for portal vein thrombosis

Ann Hematol. 2006 Feb;85(2):126-8. doi: 10.1007/s00277-005-0020-1. Epub 2005 Nov 10.

Abstract

Prothrombin G20210A gene variant has been found in 0-23% of patients with portal vein thrombosis (PVT). This wide variation makes it difficult to assess the importance of prothrombin G20210A gene variant as a predisposing factor for PVT. In this study from South India, none of the patients with idiopathic PVT (0/38) or any of the controls (0/46) had prothrombin G20210A gene variant. Prothrombin G20210A gene variant does not contribute to the development of PVT in India.

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Female
  • Genetic Variation*
  • Humans
  • India
  • Infant
  • Male
  • Middle Aged
  • Polymorphism, Genetic*
  • Portal Vein / pathology*
  • Prothrombin / genetics*
  • Venous Thrombosis / etiology
  • Venous Thrombosis / genetics*

Substances

  • Prothrombin

Associated data

  • OMIM/176930