NR AMAZ
AU Vingerhoets,F.J.; Hegyi,I.; Aguzzi,A.; Myers,P.; Pizzolato,G.; Landis,T.
TI An unusual case of Creutzfeldt-Jakob disease
QU Neurology 1998 Aug; 51(2): 617-9
PT journal article
AB A patient with histopathologically verified sporadic Creutzfeldt-Jakob disease (CJD) presented initially with diplopia, sleep disturbances, and L-dopa-responsive parkinsonism. After more than a year of slow progression, he did not become demented, and failed to fulfill the clinical criteria for possible CJD. No clinical examinations currently proposed to detect CJD showed the disease. CJD should be in the differential diagnosis of "parkinson plus" syndromes until a different etiology has been found or a histopathologic examination performed.
MH Case Report; Creutzfeldt-Jakob Syndrome/*pathology; Diagnosis, Differential; Disease Progression; Human; Male; Middle Age; Parkinson Disease/*pathology; *Periodicity; Support, Non-U.S. Gov't
AD Clinic of Neurology, University Hospital of Geneva, Switzerland.
SP englisch
PO USA