Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Inherited neurodegenerative disorder · Movement disorder · Creutzfeldt Jacob disease
Inherited Creutzfeldt-Jakob disease
Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia.
This condition has no sub-types.