Late-onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation

Ann Neurol. 2002 Apr;51(4):525-30. doi: 10.1002/ana.10163.

Abstract

We report a case of frontotemporal dementia and parkinsonism linked to chromosome 17 of 5 years' duration in an 81-year-old man whose brother had died at age 86 years with dementia. In this patient, we found frontal and temporal neuronal loss, glial-predominant tau deposits, progressive supranuclear palsy-like straight tubules, accumulation of 4-repeat-predominant Sarkosyl-insoluble tau, and a novel exon 1 (Arg5His) tau gene mutation. This mutation decreased microtubule-promoting capacity and increased fibrillation of tau in vitro. Thus, we consider that the Arg5His mutation is an authentic tau gene abnormality responsible for the patient's tau pathology and late-onset dementia.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age of Onset
  • Aged
  • Aged, 80 and over
  • Dementia / genetics*
  • Dementia / pathology
  • Detergents
  • Exons
  • Humans
  • Inclusion Bodies / pathology
  • Inclusion Bodies / ultrastructure
  • Male
  • Microscopy, Electron
  • Microtubules / metabolism
  • Microtubules / pathology
  • Oligodendroglia / pathology
  • Oligodendroglia / ultrastructure
  • Point Mutation*
  • RNA, Messenger / analysis
  • Sarcosine / analogs & derivatives*
  • Solubility
  • tau Proteins / genetics*
  • tau Proteins / metabolism

Substances

  • Detergents
  • RNA, Messenger
  • tau Proteins
  • sarkosyl
  • Sarcosine