Early-onset, rapidly progressive familial tauopathy with R406W mutation

Neurology. 2002 Mar 12;58(5):811-3. doi: 10.1212/wnl.58.5.811.

Abstract

An early-onset and rapidly progressive familial tauopathy with R406W mutation is described. The patient was a 47-year-old man who first presented with psychiatric symptoms followed by overt dementia at age 52 and died 1 year later. Postmortem study revealed tangle-associated neuronal degeneration, accentuated in the medial temporal lobe. R406W mutation was determined by sequence analysis and immunocytochemically with anti-mutant tau antibody.

Publication types

  • Case Reports

MeSH terms

  • Age of Onset
  • Dementia / etiology
  • Dementia / pathology*
  • Disease Progression
  • Hippocampus / pathology
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Mutation
  • Neurofibrillary Tangles / pathology
  • Tauopathies / genetics*
  • Tauopathies / pathology*
  • Tauopathies / physiopathology
  • Temporal Lobe / pathology
  • tau Proteins / genetics*

Substances

  • tau Proteins