Article
Clinical features of sporadic fatal insomnia.
Reviews in neurological diseases - 1 Jan 2009
Barash Jed A
Abstract excerpt
Recent advances in neuropathology, genotyping, and physiochemical characterization of proteins have allowed for the classification and verification of MM2-thalamic Creutzfeldt-Jakob disease (CJD). CJD is a fatal neurodegenerative illness belonging to the transmissible spongiform encephalopathies, also known as prion diseases. Sporadic CJD is generally classified by the genotype at codon 129 of the prion protein...
Topics
- Adult
- Aged
- Creutzfeldt-Jakob Syndrome
- Diagnosis, Differential
- Disease Progression
- Female
- Genetic Predisposition to Disease
- Humans
- Insomnia, Fatal Familial
- Male
- Middle Aged
- Mutation
- PrPSc Proteins
- Predictive Value of Tests
- Radionuclide Imaging
- Thalamic Diseases
- Thalamus
