Parkinsonism can result from numerous causes (1). Postinfectious etiologies are rare today but were common in the past. Postencephalitic parkinsonism was one of the most dramatic sequelae of encephalitis lethargica (von Economo's disease). This epidemic began in 1916-1917 in Austria, and cases had b
Movement disorders associated with encephalitis lethargica: A video compilation
β Scribed by Joel A. Vilensky; Christopher G. Goetz; Sid Gilman
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 164 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Encephalitis lethargica (EL; epidemic encephalitis; von Economo's disease) often presented with a movement disorder, and the motor consequences of postencephalitic parkinsonism (PEP) were characteristic of the chronic sequelae of this condition. PEP was similar to Parkinson's disease but was more variable and had some distinct features such as oculogyric crises. Although two previous publications have included video images of the movement disorders associated with EL and PEP, the sequences presented were typically short, showed only a few patients, and did not include the work of several neurologists who had the foresight to preserve filmed images of their patients. We describe the most complete record of EL and PEP moving images that have been preserved and make them available in edited form. Β© 2005 Movement Disorder Society
π SIMILAR VOLUMES
## Abstract A 48βyearβold man presented with a progressive gait disorder. He had longstanding ataxia, oculomotor apraxia, motor delay, and cognitive impairment, diagnosed as cerebral palsy. Physical examination revealed ataxia, oculomotor apraxia, extrapyramidal signs, and a wideβbased, shuffling g
## Abstract Glutaric aciduria type 1 (GA1) is an autosomal recessive neurometabolic disorder due to glutaryl CoA dehydrogenase deficiency. Comprehensive descriptions of GA1βassociated movement disorders are rare. In order to refine the description of the motor phenotype, we prospectively studied 16
Kasabach-Merritt syndrome (KMS) is a severe vascular growth disorder associated with generalized kaposiform hemangioendotheliomas, tufted angiomas, consumptive coagulopathy, and thrombocytopenia. [1][2][3] Since the initial report, 1 case series have addressed its complex pathophysiology and treatme
## Abstract The aim of this study was to define the clinical characteristics of patients who developed movement disorders in association with moyamoya disease (MMD). Using PubMed and medical records of our hospital from 1985 to 2008, we searched for patients who developed movement disorders in asso