Brief Report with Video
Neuronal intranuclear inclusion disease: Report on a case originally diagnosed as dopa-responsive dystonia with Lewy bodies
Version of Record online: 17 JUN 2005
Copyright © 2005 Movement Disorder Society
Volume 20, Issue 10, pages 1345–1349, October 2005
How to Cite
Paviour, D. C., Revesz, T., Holton, J. L., Evans, A., Olsson, J.-E. and Lees, A. J. (2005), Neuronal intranuclear inclusion disease: Report on a case originally diagnosed as dopa-responsive dystonia with Lewy bodies. Mov. Disord., 20: 1345–1349. doi: 10.1002/mds.20559
- Issue online: 4 OCT 2005
- Version of Record online: 17 JUN 2005
- Manuscript Accepted: 20 JAN 2005
- Manuscript Received: 10 DEC 2004
- PSP (Europe) Association
This article includes Supplementary Video, available online at http://www.interscience.wiley.com/jpages/0885-3185/suppmat .
|jws-mds.20559.mpg||13604K||Segment 1: Patient at approx. 12 years of age. Myopathic facies with bilateral ptosis, difficulty with eyelid opening and facial hypomimia. Intermittent tongue tremor and postural tremor of the hands. Segment 2: Patient at approx. 18 years of age. Reduced arm swing when walking, asymmetrical impairment of fine finger movements (left worse than right). Bilateral ptosis. Segment 3: Patient in her early 20?s. Impairment mobility requiring a walker to move safely. Lower limb dystonia is present. Retrocollis and facial dystonia. Severe postural instability with spontaneous loss of balance. This video presentation has been abbreviated. The full version will appear on theMovementDisorders DVD Supplement, which is issued bi-annually.|
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