New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome

Brain Res Mol Brain Res. 1995 Jun;30(2):385-8. doi: 10.1016/0169-328x(95)00034-p.

Abstract

We found novel variants in the open reading frame of the prion protein (PrP) gene in a family with Gerstmann-Sträussler syndrome (GSS). Codon 219Lys variant is a normal polymorphism which we found recently. Some GSS cases were identified with codon 102 mutation (proline to leucine) and codon 219Lys polymorphism. While two families had a codon 102 mutation and codon 219Lys polymorphism in different alleles, 4 patients in one family had both in the same allele. The clinicopathological features of these 4 patients were clearly different from previously reported GSS patients with codon 102 mutation. These cases should be reported as a new variant of GSS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Family
  • Female
  • Gene Expression
  • Gerstmann-Straussler-Scheinker Disease / genetics*
  • Gerstmann-Straussler-Scheinker Disease / metabolism
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Mutation
  • Pedigree
  • Polymerase Chain Reaction
  • Prions / genetics*
  • Prions / metabolism

Substances

  • Prions