Creutzfeldt-Jakob disease (CJD).This rare form of dementia happens when a protein, called a prion, folds into an abnormal shape, and other proteins start to do the same. This damages brain cells and triggers a fast mental decline.
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The median survival in sCJD is 5 months, with 90% of patients dying within 1 year [1, 4, 10, 14-16]. An Evaluation of Rapidly Progressive Dementia Culminating in a Diagnosis of Creutzfeldt-Jakob Disease This case highlights an unusual presentation of sCJD characterised by a rapidly progressiv...
Down syndrome is the foremost common genetic cause of intellectual disability. The additional copy of chromosome 21 confers potential changes in virtually all organ systems, including the brain, neck structures, and spine. Neuroradiologists should be aware of the multitude of imaging\nfindings in ...
Gerstmann-Straussler-Scheinker (GSS) disease is manifested as a very unsteady gait plus other signs of damage to the cerebellum - a specific area of the brain. The symptoms are very much like CJD. GSS is also fatal. Fatal familial insomnia in which dementia follows difficulty sleeping. ...
(CJD) is a kind of human prion disease with progressive dementia and cerebellar dysfunction appearing as muscular incoordination, visual, speech, and gait clinical symptoms [73]. The CoV-2 disease might induce an exacerbated, faster pathogenesis and manifestations of CJD, as well as decreased ...