Clinical phenotypes of progressive aphasia

Stefano F. Cappa, Maria Luisa Gorno-Tempini

Research output: Contribution to journalArticle

Abstract

Primary progressive aphasia is defined as an insidious, gradual impairment of language function, which is not accompanied by other cognitive disorders for at least 2 years after onset, and which can be due to a number of neurodegenerative disorders, such as the different varieties of frontotemporal dementia or Alzheimer's disease. The clinical presentations are heterogeneous, as they faithfully reflect the preferential location of pathological involvement within the language networks. A careful definition of the clinical phenotypes of primary progressive aphasia is contributing to the understanding of language organization in the brain. Moreover, the predictive value of the clinical phenotype as to the underlying pathology has important implications for clinical trials of disease-modifying drugs.

Original languageEnglish
Pages (from-to)153-160
Number of pages8
JournalFuture Neurology
Volume4
Issue number2
DOIs
Publication statusPublished - 2009

Keywords

  • Dementia
  • Language
  • Pick's disease
  • Progranulin
  • Tauopathies

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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