Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism

Parkinsonism Relat Disord. 2018 Oct;55:145-147. doi: 10.1016/j.parkreldis.2018.06.006. Epub 2018 Jun 6.
No abstract available

Keywords: Behavior; Dementia; Frontotemporal dementia; Neuropsychiatry; PARK2; Parkinsonism; Psychiatry.

Publication types

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

MeSH terms

  • Fluorodeoxyglucose F18 / pharmacokinetics
  • Humans
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Parkinsonian Disorders / diagnostic imaging
  • Parkinsonian Disorders / genetics*
  • Phenotype
  • Positron-Emission Tomography
  • Ubiquitin-Protein Ligases / genetics*

Substances

  • Fluorodeoxyglucose F18
  • Ubiquitin-Protein Ligases
  • parkin protein