Familial Creutzfeldt-Jakob disease with M232R mutation presented with corticobasal syndrome

Neurol Sci. 2015 Jul;36(7):1291-3. doi: 10.1007/s10072-014-2038-4. Epub 2014 Dec 17.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • 14-3-3 Proteins / cerebrospinal fluid
  • Aged
  • Arginine / genetics
  • Basal Ganglia / pathology
  • Brain Diseases / pathology*
  • Brain Diseases / physiopathology*
  • Cerebral Cortex / pathology
  • Creutzfeldt-Jakob Syndrome / diagnosis*
  • Creutzfeldt-Jakob Syndrome / genetics*
  • DNA Mutational Analysis
  • Female
  • Humans
  • Methionine / genetics
  • Mutation / genetics*
  • Prions / genetics*

Substances

  • 14-3-3 Proteins
  • Prions
  • Arginine
  • Methionine