A parkinsonian movement disorder with brain iron deposition and a haemochromatosis mutation

J Neurol. 2013 Aug;260(8):2170-1. doi: 10.1007/s00415-013-6995-y. Epub 2013 Jun 23.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Brain / pathology
  • Brain Chemistry / genetics
  • Brain Chemistry / physiology
  • DNA / genetics
  • Fatal Outcome
  • Female
  • Hemochromatosis / genetics*
  • Hemochromatosis / pathology
  • Humans
  • Iron / metabolism*
  • Middle Aged
  • Multiple System Atrophy / etiology
  • Multiple System Atrophy / genetics
  • Mutation / genetics
  • Mutation / physiology
  • Parkinsonian Disorders / genetics*
  • Parkinsonian Disorders / metabolism*
  • Parkinsonian Disorders / pathology

Substances

  • DNA
  • Iron