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Signs and symptoms are classified into three groups based on the affected functions of the frontal and temporal lobes: [8] These are behavioural variant frontotemporal dementia, semantic dementia, and progressive nonfluent aphasia. An overlap between symptoms can occur as the disease progresses and spreads through the brain regions.
After symptoms arise, the average life expectancy is seven to 13 years. ... are diagnosed with behavioral-variant frontotemporal dementia. Because the disease destroys cells in key parts of the ...
The term young onset dementia is becoming more widely used to avoid the potential confusion between early onset dementia and early stage dementia. This term is now used as presenile dementia which is a historical term of people diagnosed with dementia from a younger age of 51 years old. This is caused by an atypical arteriosclerosis of the brain.
The three clinical subtypes of frontotemporal lobar degeneration, frontotemporal dementia, semantic dementia and progressive nonfluent aphasia, are characterized by impairments in specific neural networks. [17] The first subtype, frontotemporal dementia, mainly affects a frontomedian network and impairs social cognition.
Frontotemporal dementia can be hard to diagnose because while dementia can be part of the illness, it's not a factor in all cases. Frontotemporal dementia can be hard to diagnose because while ...
There are two types of FTD – behavioural variant FTD (bvFTD) and primary progressive aphasia (PPA). BvFTD, which results from damage to the frontal lobes of the brain, mainly causes problems ...
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