A new point mutation of the PRNP gene in Gerstmann-Sträussler-Scheinker case in Poland

Folia Neuropathol. 2000;38(4):164-6.

Abstract

We report here a case of Gerstmann-Sträussler-Scheinker (GSS) disease with a new mutation at the codon 232 (Met to Thr) of the PRNP gene. This case was characterized by PrP-immunopositive kuru and multicentric plaques; these plaques were also seen in the cerebral cortex, hippocampus and in the deep subcortical nuclei. Diffuse PrP depositions were also detected. In the temporal cortex, a few plaques were immunopositive for both PrP and Abeta; the latter was expressed at the periphery of the PrP-immunopositive cores. This mutation was absent from 40 healthy Polish controls and from 16 other Polish CJD cases, and we therefore believe that 232Thr is a new pathogenic mutation and not a benign polymorphism.

Publication types

  • Case Reports

MeSH terms

  • Amino Acid Substitution*
  • Amyloid / genetics*
  • Codon / genetics
  • DNA Mutational Analysis
  • Gerstmann-Straussler-Scheinker Disease / genetics*
  • Humans
  • Male
  • Middle Aged
  • Point Mutation*
  • Poland
  • Prion Proteins
  • Prions
  • Protein Precursors / genetics*

Substances

  • Amyloid
  • Codon
  • PRNP protein, human
  • Prion Proteins
  • Prions
  • Protein Precursors