A novel L266V mutation of the tau gene causes frontotemporal dementia with a unique tau pathology

Ann Neurol. 2003 Jan;53(1):133-7. doi: 10.1002/ana.10447.

Abstract

We report a novel mutation of tau (L266V missense mutation in exon 9) which may cause a type of familial frontotemporal dementia. The brain of a patient showed Pick body-like inclusions and unique tau-positive, argyrophilic astrocytes with stout filaments and naked, round, or irregular argyrophilic inclusions with deposits of both three-repeat and four-repeat tau. Recombinant tau with a L266V mutation showed a reduced ability to promote microtubule assembly, which may be the primary effect of the mutation.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Astrocytes / pathology
  • Dementia / genetics*
  • Dementia / pathology*
  • Humans
  • Inclusion Bodies / pathology
  • Male
  • Mutation, Missense*
  • Neurons / pathology
  • tau Proteins / genetics*

Substances

  • tau Proteins