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Article

Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review

22 Oct 2010

Abstract excerpt

Frontotemporal dementia (FTD) is the second most common young-onset dementia and is clinically characterised by progressive behavioural change, executive dysfunction and language difficulties. Three clinical syndromes, behavioural variant FTD, semantic dementia and progressive non-fluent aphasia, form part of a clinicopathological spectrum named frontotemporal lobar degeneration (FTLD). The classical...

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PMID: 20971753
DOI: 10.1136/jnnp.2010.212225

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