Motor neuron disease-frontotemporal dementia: a clinical continuum

Expert Rev Neurother. 2015 May;15(5):509-22. doi: 10.1586/14737175.2015.1034108. Epub 2015 Apr 11.

Abstract

Overlap between motor neuron disease (MND) and frontotemporal dementia (FTD) occurs at clinical, genetic and pathological levels, and has been recently strengthened through the discovery of the C9orf72 genetic expansion. MND is now considered to be a multisystem disorder in which cognitive involvement may be present and, in some cases, may evolve to frank FTD. Identifying cognitive features in MND can be challenging, while, similarly, motor dysfunction in FTD may be overlooked. As such, the present review aims to decipher the variety of overlapping clinical features across the MND-FTD continuum.

Keywords: C9orf72; Frontotemporal dementia; behavior; clinical continuum; cognition; genetics; motor neuron disease; neuroimaging; neurophysiology.

Publication types

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

MeSH terms

  • Animals
  • C9orf72 Protein
  • Cognition / physiology*
  • Frontotemporal Dementia / diagnosis
  • Frontotemporal Dementia / genetics
  • Frontotemporal Dementia / therapy*
  • Humans
  • Motor Neuron Disease / diagnosis
  • Motor Neuron Disease / genetics
  • Motor Neuron Disease / therapy*
  • Mutation / genetics
  • Phenotype*
  • Proteins / genetics

Substances

  • C9orf72 Protein
  • C9orf72 protein, human
  • Proteins