Essential myoclonus and myoclonus dystonia
β Scribed by Dr. Niall P. Quinn
- Book ID
- 102947392
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 561 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
This review explores the history and use of the terms essential myoclonus and myoclonie dystonia. In addition, the review proposes that herediatry essential myoclonus and dominantly inherited myoclonic dystonia, with lightning jerks and dramatic response to alcohol, are the same disease, although proof of this hypothesis must come from ongoing genetic studies.
π SIMILAR VOLUMES
## Abstract Our knowledge of the clinical, neurophysiological, and genetic aspects of myoclonusβdystonia (MβD) has improved markedly in the recent years. Basic research has provided new insights into the complex dysfunctions involved in the pathogenesis of MβD. On the basis of a comprehensive liter
From a family with essential familial myoclonus, 150 members in eight generations were studied. Twenty-five of them suffered from myoclonus of varying severity. The findings in routine examinations of blood, urine and cerebrospinal fluid, EEG and skull radiographs were normal. Therapeutic trials did
## Abstract Inherited myoclonusβdystonia (MβD) is an autosomal dominant disorder characterized by myoclonus and dystonia that often improves with alcohol. To examine the electrophysiologic characteristics of MβD, we studied 6 patients from 4 different families and 9 ageβmatched healthy subjects. Ne