Co-segregation of the PROS1 locus and protein S deficiency in families having no detectable mutations in PROS1

J Thromb Haemost. 2004 Nov;2(11):1918-23. doi: 10.1111/j.1538-7836.2004.00950.x.

Abstract

Inherited deficiency of protein S constitutes an important risk factor of venous thrombosis. Many reports have demonstrated that causative mutations in the protein S gene are found only in approximately 50% of the cases with protein S deficiency. It is uncertain whether the protein S gene is causative in all cases of protein S deficiency or if other genes are involved in cases where no mutation is identified. The aim of the current study was to determine whether haplotypes of the protein S gene cosegregate with the disease phenotype in cases where no mutations have been found. Eight protein S-deficient families comprising 115 individuals where previous DNA sequencing had failed to detect any causative mutations were analyzed using four microsatellite markers in the protein S gene region. Co-segregation between microsatellite haplotypes and protein S deficiency was found in seven of the investigated families, one family being uninformative. This suggests that the causative genetic defects are located in or close to the protein S gene in a majority of such cases where no mutations have been found.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Mutational Analysis
  • Family Health
  • Female
  • Haplotypes
  • Humans
  • Inheritance Patterns*
  • Lod Score
  • Male
  • Microsatellite Repeats
  • Mutation
  • Pedigree
  • Protein S / genetics*
  • Protein S Deficiency / genetics*

Substances

  • Protein S