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Geriatric medicine

Frontotemporal dementia

Recognising behavioural variant FTD and the primary progressive aphasias, the Rascovsky criteria, why the MMSE and early MRI can be normal, separating FTD from late-onset psychiatric illness, the MND overlap, why cholinesterase inhibitors don't help, SSRIs and trazodone, and young-onset supports in Australia.

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At a glance

  • A group of neurodegenerative syndromes from frontotemporal lobar degeneration (tau, TDP-43 or FUS). Pathology and genetics (C9orf72, GRN, MAPT) are in Pathophysiology of non-Alzheimer dementias.
  • A leading cause of young-onset dementia, with peak onset between 45 and 65. A quarter or so start after 65, where it is easily called Alzheimer disease or late-onset depression.
  • Behaviour, personality or language fails first. Memory and visuospatial function are relatively spared early, the reverse of Alzheimer disease.

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Sources

Last updated
14 November 2026
What changed
  • 14 November 2026 Personal emails, About story and Australian-style copy

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