Factor V Q 506 mutation in children with thrombosis

Am J Hematol. 1996 Sep;53(1):37-9. doi: 10.1002/(SICI)1096-8652(199609)53:1<37::AID-AJH8>3.0.CO;2-6.

Abstract

The factor V Leiden mutation in 12-children with thrombosis and in 20 controls was investigated. Five heterozygous individuals and 1 homozygous individual among the cases with thrombosis and 1 heterozygous individual among controls were found. Central nervous system thromboses were increased in children with the factor V mutation, associated with protein S deficiency.

MeSH terms

  • Case-Control Studies
  • Child
  • Factor V / genetics*
  • Female
  • Heterozygote
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Mutation*
  • Protein S Deficiency / genetics
  • Thrombosis / genetics*

Substances

  • Factor V