Diagnosis of Creutzfeldt-Jakob disease is difficult because the condition resembles many other neurodegenerative diseases. A new test is now available that can detect minute quantities of the CJD-specific abnormal prion protein from all subtypes of sporadic CJD in cerebral spinal fluid or nasal mucosa. More here and here.
News from NORD
New Definitive Diagnostic Test for Creutzfeldt-Jakob Disease Is Available
Publish date: February 15, 2017