## Abstract Nonmotor symptoms (NMS) are increasingly recognized as a significant cause of morbidity in later stages of Parkinson's disease (PD). Prodromal NMS are also a well recognized component of the clinical picture in some patients but the prevalence of NMS as presenting complaints, and their
Binswanger's disease presenting as levodopa-responsive parkinsonism: Clinicopathologic study of three cases
β Scribed by Dr. M. H. Mark; J. I. Sage; A. S. Walters; R. C. Duvoisin; D. C. Miller
- Book ID
- 102946226
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 516 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
We report three cases of autopsyβproven Binswanger's disease (subcortical arteriosclerotic encephalopathy) with unusual clinical features. Two patients had supranuclear gaze disturbances, early gait dysfunction, and speech disorders suggestive of progressive supranuclear palsy. One of these patients was not demented at the time of death. The third patient had features typical of Parkinson's disease. All three patients were responsive to treatment with levodopa. The clinical spectrum of Binswanger's disease should be expanded to include levodopaβresponsive parkinsonism.
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