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Genetic Creutzfeldt-Jakob disease mimicking dementia with Lewy bodies: Clinical and radiological findings

It is important to distinguish Creutzfeldt-Jakob disease (CJD) from other rapidly progressive dementia disorders to provide appropriate clinical care and prevent iatrogenic transmission. However, the differentiation between patients with CJD (there are sporadic [sCJD], acquired, and genetic CJD [gCJD]) and those with Alzheimer's disease and dementia with Lewy bodies (DLB), the two main causes of neurodegenerative dementia among elderly people, is sometimes difficult, especially in the early stages [1,2].

from Journal of the Neurological Sciences https://ift.tt/2rDGzV2
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