Creutzfeldt-Jakob disease presenting as progressive supranuclear palsy

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

Progressive supranuclear palsy (PSP) is a neurodegenerative disorder characterized by an akinetic rigid syndrome with vertical supranuclear ophthalmoplegia, early falls, and levodopa resistance. The pathological substrate of PSP consists of filamentous tau degenerative lesions affecting neurons and glia. Other disorders can present with a similar clinical picture, most commonly corticobasal degeneration and multiple system atrophy. Non-neurodegenerative disorders are rare causes of the PSP syndrome. In this report we describe clinical and pathological features of two cases of Creutzfeldt- Jakob disease (CJD) presenting with the PSP syndrome and discuss which features may help prevent misdiagnosis. To our knowledge, this is the first report of cases of CJD with autopsy confirmation that presented with a PSP syndrome.

Original languageEnglish (US)
Pages (from-to)343-346
Number of pages4
JournalEuropean Journal of Neurology
Volume11
Issue number5
DOIs
StatePublished - May 2004

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Progressive Supranuclear Palsy
Creutzfeldt-Jakob Syndrome
Multiple System Atrophy
Ophthalmoplegia
Levodopa
Diagnostic Errors
Neuroglia
Neurodegenerative Diseases
Autopsy
Neurons

Keywords

  • Creutzfeldt-Jakob disease
  • Progressive supranuclear palsy
  • Vertical supranuclear ophthalmoplegia

ASJC Scopus subject areas

  • Clinical Neurology
  • Neuroscience(all)

Cite this

Creutzfeldt-Jakob disease presenting as progressive supranuclear palsy. / Josephs, Keith Anthony; Tsuboi, Y.; Dickson, Dennis W.

In: European Journal of Neurology, Vol. 11, No. 5, 05.2004, p. 343-346.

Research output: Contribution to journalArticle

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