Abstract
AbstractHere, we review recent progress in the diagnosis and management of primary progressive aphasia—the language-led dementias. We pose six key unanswered questions that challenge current assumptions and highlight the unresolved difficulties that surround these diseases. How many syndromes of primary progressive aphasia are there—and is syndromic diagnosis even useful? Are these truly ‘language-led’ dementias? How can we diagnose (and track) primary progressive aphasia better? Can brain pathology be predicted in these diseases? What is their core pathophysiology? In addition, how can primary progressive aphasia best be treated? We propose that pathophysiological mechanisms linking proteinopathies to phenotypes may help resolve the clinical complexity of primary progressive aphasia, and may suggest novel diagnostic tools and markers and guide the deployment of effective therapies.
Funder
Invention for Innovation Programme
Wellcome Institutional Strategic Support Fund
NIHR Advanced Fellowship
Medical Research Council
National Institute for Health Research Rare Disease Translational Research Collaboration
Royal National Institute for Deaf People
Wellcome Trust
Alzheimer’s Society
Alzheimer’s Research UK
UK Dementia Research Institute
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Cited by
11 articles.
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