TARDBP mutation associated with semantic variant primary progressive aphasia, case report and review of the literature

Neurocase. 2018 Oct-Dec;24(5-6):301-305. doi: 10.1080/13554794.2019.1581225. Epub 2019 Feb 16.

Abstract

Semantic variant primary progressive aphasia (svPPA) is a clinical syndrome included in the frontotemporal dementia (FTD) spectrum. Unlike other forms of FTD, it is sporadic in the majority of cases and not commonly associated with motor neuron disease (MND). We describe a case of svPPA associated with MND in the same family, due to a mutation of the transactive response DNA binding protein (TARDBP) gene, and review the literature.

Keywords: Semantic variant PPA; TARDBP mutation; TDP-43; genetics; motor neuron disease.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Aphasia, Primary Progressive / diagnostic imaging
  • Aphasia, Primary Progressive / genetics*
  • Aphasia, Primary Progressive / physiopathology*
  • DNA-Binding Proteins / genetics*
  • Female
  • Humans
  • Middle Aged
  • Motor Neuron Disease / genetics
  • Mutation
  • Pedigree
  • Semantics

Substances

  • DNA-Binding Proteins
  • TARDBP protein, human