Familial Creutzfeldt-Jakob disease with E200K mutation presenting with neurosensorial hypoacusis

J Neurol Neurosurg Psychiatry. 2007 Jan;78(1):103-4. doi: 10.1136/jnnp.2006.095588.
No abstract available

Publication types

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

MeSH terms

  • Creutzfeldt-Jakob Syndrome / complications*
  • Creutzfeldt-Jakob Syndrome / genetics*
  • Deafness / etiology*
  • Humans
  • Male
  • Middle Aged
  • Mutation
  • Pedigree
  • Polyneuropathies / etiology*
  • Prions / genetics

Substances

  • Prions