A case of sporadic Creutzfeldt-Jakob disease
Sporadic Creutzfeldt-Jakob disease (CJD) is a very rare and fatal disease caused by prions – proteins with unique characteristics and infective potential. The typical clinical presentation is of a rapidly progressive dementia with myoclonus, cerebellar, pyramidal, extra pyramidal and visual signs. T...
| Main Authors: | , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Amaltea Medical Publishing House
2012-06-01
|
| Series: | Romanian Journal of Neurology |
| Subjects: | |
| Online Access: | https://rjn.com.ro/articles/2012.2/RJN_2012_2_Art-05.pdf |