Late onset thrombosis in a case of severe protein S deficiency due to compound heterozygosity for PROS1 mutations

J Thromb Haemost. 2008 Jul;6(7):1235-7. doi: 10.1111/j.1538-7836.2008.02994.x. Epub 2008 Jul 1.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Blood Proteins / deficiency*
  • Blood Proteins / genetics
  • Child
  • Child, Preschool
  • DNA Mutational Analysis
  • Family Health
  • Female
  • Heterozygote
  • Humans
  • Infant
  • Male
  • Mutation
  • Protein S
  • Protein S Deficiency / complications*
  • Protein S Deficiency / genetics
  • Thrombosis / etiology*
  • Thrombosis / genetics

Substances

  • Blood Proteins
  • PROS1 protein, human
  • Protein S