Slowly progressive behavioral frontotemporal dementia with C9orf72 mutation. Case report and review of the literature

Neurocase. 2018 Feb;24(1):68-71. doi: 10.1080/13554794.2018.1428353. Epub 2018 Jan 22.

Abstract

We present a 86-year-old woman without relevant medical history and two brothers who died by dementia, who started at 55 years with depression and personality changes with ongoing worsening (>30 years) and functional decline. Screening dementia blood test and brain magnetic resonance imaging did not show results that pointed to a secondary cause. The patient met the diagnostic criteria for possible behavioral frontotemporal dementia with a slow progression (bvFTD-SP), suggesting a benign variant. A genetic study confirmed a C9ORF72 hexanucleotide expansion, making this the sixth case mentioned in the literature. We review and discuss the other cases described previously.

Keywords: C9orf72 gene; Slowly progressive behavioral frontotemporal dementia; dementia; genetics; hexanucleotide expansion.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Aged, 80 and over
  • C9orf72 Protein / genetics*
  • Disease Progression
  • Female
  • Frontotemporal Dementia / genetics*
  • Humans
  • Mutation / genetics*

Substances

  • C9orf72 Protein
  • C9orf72 protein, human