Neurodegenerative disorders with extensive tau pathology

A comparative study and review

Mel B. Feany, Dennis W Dickson

Research output: Contribution to journalArticle

240 Citations (Scopus)

Abstract

Many neurodegenerative disorders with onset in mid to late adult life present diagnostic challenges to clinicians and pathologists alike. A distinguishing neuropathological feature has traditionally been the presence or absence of neurofibrillary tangles. Recent biochemical and molecular biological studies have identified the microtubule-binding protein tau as the predominant component of these and related inclusions, and have provided powerful new reagents for the study of neurodegenerative diseases. Several diseases previously considered distinct pathophysiological entities contain similar tau-immunoreactive lesions, but qualitative and regional anatomical differences in vulnerability can differentiate the disorders. Comparison of tau-immunoreactive lesions in three relatively uncommon neurodegenerative diseases - progressive supranuclear palsy, Pick's disease, and corticobasal degeneration - illustrates the types of analyses that demonstrate unexpected pathological similarities, but also fundamental differences between these disorders. These results have important implications for the differential diagnosis of disorders containing tau-immunoreactive lesions, including Alzheimer's disease.

Original languageEnglish (US)
Pages (from-to)139-148
Number of pages10
JournalAnnals of Neurology
Volume40
Issue number2
StatePublished - Aug 1996
Externally publishedYes

Fingerprint

Neurodegenerative Diseases
Pathology
Pick Disease of the Brain
Microtubule Proteins
Progressive Supranuclear Palsy
Neurofibrillary Tangles
Carrier Proteins
Alzheimer Disease
Differential Diagnosis
Pathologists

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Neurodegenerative disorders with extensive tau pathology : A comparative study and review. / Feany, Mel B.; Dickson, Dennis W.

In: Annals of Neurology, Vol. 40, No. 2, 08.1996, p. 139-148.

Research output: Contribution to journalArticle

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