Literature DB >> 6322950

An atypical case of progressive supranuclear palsy.

A J Gomori, A A Sima.   

Abstract

We report a 59 year old woman who presented with double vision, nuchal pain and mild dementia. On neurological examination she demonstrated third, sixth and seventh nerve palsies and ataxia. Following intravenous ACTH and oral prednisone therapy she showed a remarkable recovery which left her with only a left facial weakness. She remained well for two years. She then developed bulbar palsy and profound dementia. Pathological examination revealed progressive supranuclear palsy (PSP). This patient demonstrated a greater variability in the course of PSP than has previously been recognized.

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Year:  1984        PMID: 6322950     DOI: 10.1017/s0317167100045315

Source DB:  PubMed          Journal:  Can J Neurol Sci        ISSN: 0317-1671            Impact factor:   2.104


  4 in total

Review 1.  Corticonigral degeneration with neuronal achromasia and basal neurofibrillary tangles.

Authors:  W Paulus; M Selim
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

2.  Progressive supranuclear palsy with Lewy bodies.

Authors:  H Mori; M Yoshimura; M Tomonaga; H Yamanouchi
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

3.  Substructure of 20 nm filaments of progressive supranuclear palsy.

Authors:  V Montpetit; D F Clapin; A Guberman
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

4.  Allocortical neurofibrillary changes in progressive supranuclear palsy.

Authors:  H Braak; K Jellinger; E Braak; J Bohl
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

  4 in total

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