Neurology: 1 case of long-term survival of exudable kerya disease.

A 63-year-old woman with slow onset dementia.
electroencephalogram suggests periodic sharp slow composite waves.
MRI visible cortical ribbon signs and substrate section high signals (Figure A-H).
genetic tests confirmed the purity of methionine (methionine) at 129 polymorphic cophers of the PRNP gene.
34 months after the onset of the disease, the patient is still alive and has not yet reached in motionless silence.
-time vibration-induced conversion tested positive for dermatic prion virus (Figure I).
the case is a rare long-lived exudable cretactic disease (Creutzfeldt-Jakob disease), which contradicts the traditional course of the disease and confirms the effectiveness of minimally invasory skin biopsies that confirm the disease before death.
(Figure: MRI performance of the central small leaves (A-D) and substrate sections (E-H) at different times after the oncology; high-signal lesions were initially confined to the rear top leaf and gradually extended to the front top leaf; I: real-time vibration-induced conversion detection of prions: positive in 4 repeat holes)