Semantic dementia associated with mutation V363I in the tau gene

J Neurol Sci. 2010 Sep 15;296(1-2):112-4. doi: 10.1016/j.jns.2010.06.007. Epub 2010 Jul 3.

Abstract

A 46-year-old woman who presented with prosopagnosia was clinically evaluated. Results of neuropsychological measures showed severe impairment in oral naming with anomia and a marked deficit in naming and recognition of famous faces. The clinical diagnosis was semantic dementia (SD). Genetic testing revealed a missense mutation V363I in exon 12 of the microtubule-associated protein tau (MAPT) gene. This is the description of an association between a mutation in the MAPT gene and a case of SD. The same mutation was recently described in a case of progressive non-fluent aphasia, but the prominent presenting feature in tau gene mutation cases is the behavioral variant of frontotemporal dementia, with typical symmetrical frontotemporal atrophy.

Publication types

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

MeSH terms

  • DNA / genetics
  • Female
  • Frontotemporal Lobar Degeneration / genetics*
  • Frontotemporal Lobar Degeneration / psychology
  • Humans
  • Middle Aged
  • Mutation / genetics
  • Mutation / physiology
  • Neuropsychological Tests
  • Prosopagnosia / genetics*
  • Prosopagnosia / psychology
  • Recognition, Psychology / physiology
  • Reverse Transcriptase Polymerase Chain Reaction
  • tau Proteins / genetics*

Substances

  • tau Proteins
  • DNA