Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease

John M Bertoni, Lorne S. Label, J. Chris Sackelleres, Samuel P. Hicks

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Seven affected individuals from three generations in a kindred having over 250 members were identified as having possible, probable, or definite Creutzfeldt-Jakob disease. Spongiform encephalopathy was found at postmortem examination in two cases. Detailed inpatient neurological examinations were performed on four of the subjects, three of whom were first observed with supranuclear gaze paralysis, gait ataxia, and rapidly progressive dementia. Supranuclear gaze paresis can be seen as an early feature of Creutzfeldt-Jakob disease, although it has been regarded as a late sign. In this, the largest reported kindred of Creutzfeldt-Jakob disease, most of the affected patients were farmers. Possible modes of infection are discussed.

Original languageEnglish (US)
Pages (from-to)618-622
Number of pages5
JournalArchives of Neurology
Volume40
Issue number10
DOIs
StatePublished - Jan 1 1983

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Creutzfeldt-Jakob Syndrome
Paralysis
Gait Ataxia
Neurologic Examination
Brain Diseases
Paresis
Dementia
Inpatients
Autopsy
Infection
Familial

ASJC Scopus subject areas

  • Arts and Humanities (miscellaneous)
  • Clinical Neurology

Cite this

Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease. / Bertoni, John M; Label, Lorne S.; Sackelleres, J. Chris; Hicks, Samuel P.

In: Archives of Neurology, Vol. 40, No. 10, 01.01.1983, p. 618-622.

Research output: Contribution to journalArticle

Bertoni, John M ; Label, Lorne S. ; Sackelleres, J. Chris ; Hicks, Samuel P. / Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease. In: Archives of Neurology. 1983 ; Vol. 40, No. 10. pp. 618-622.
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