AXILLARY ARTERY THROMBOSIS IN A NEWBORN HOMOZYGOUS FOR METHYLENETETRAHYDROFOLATE REDUCTASE (A1298C) MUTATION AND HETEROZYGOUS FOR FACTOR V LEIDEN (G506A) MUTATION

Genet Couns. 2016;27(1):87-9.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Axillary Artery / diagnostic imaging
  • Factor V / genetics*
  • Female
  • Humans
  • Infant, Newborn
  • Infant, Newborn, Diseases / diagnostic imaging
  • Infant, Newborn, Diseases / genetics*
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics*
  • Mutation
  • Thrombosis / diagnostic imaging
  • Thrombosis / genetics*
  • Ultrasonography

Substances

  • factor V Leiden
  • Factor V
  • Methylenetetrahydrofolate Reductase (NADPH2)