Progressive supranuclear palsy in a family with TDP-43 pathology

Neurocase. 2015;21(2):178-84. doi: 10.1080/13554794.2013.878729. Epub 2014 Jan 30.

Abstract

A member of a family with an autosomal dominant pattern of frontotemporal dementia (FTD) with a TDP-43 pathological substrate in other members and no mutations in FTD-associated genes developed behavioral variant FTD followed by Progressive Supranuclear Palsy. Autopsy revealed a pure tauopathy of PSP pattern.

Conclusions: The findings raise the possibility of shared pathogenic pathways and a proximal genetic abnormality between PSP and FTLD-43.

Keywords: Progressive Supranuclear Palsy; frontotemporal dementia; genetics.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural

MeSH terms

  • Brain / pathology*
  • DNA-Binding Proteins / metabolism
  • Family
  • Female
  • Frontotemporal Dementia / complications*
  • Frontotemporal Dementia / genetics
  • Frontotemporal Dementia / pathology*
  • Humans
  • Middle Aged
  • Pedigree
  • Supranuclear Palsy, Progressive / complications*
  • Supranuclear Palsy, Progressive / pathology*
  • tau Proteins / metabolism

Substances

  • DNA-Binding Proteins
  • MAPT protein, human
  • TARDBP protein, human
  • tau Proteins