Alcohol-sensitive hereditary essential myoclonus with dystonia: a study of 6 Brazilian patients

Neurol Sci. 2000 Dec;21(6):373-7. doi: 10.1007/s100720070053.

Abstract

We present the clinical profile of a group of patients with myoclonus and dystonia sensitive to alcohol and address these cases in the context of essential myoclonus. Six patients from 4 families were selected: 4 men and 2 women with myoclonus affecting predominantly the arms. Active movements of these segments elicited the dystonic and myoclonic movements. A marked improvement with alcohol intake was seen. Laboratory findings including EEG, SSEP, and cranial CT and MRI were normal. Surface EMG recording showed bursts with duration of 30-112 ms in 3 patients. One patient showed a triphasic recording pattern (agonist-antagonist-agonist) of ballistic type. Our findings suggest that the myoclonus-dystonia disorder is present in Brazilian patients.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age of Onset
  • Brain / drug effects
  • Brain / pathology
  • Brain / physiopathology
  • Brazil
  • Dystonia / complications*
  • Dystonia / genetics
  • Dystonia / physiopathology
  • Electroencephalography
  • Electromyography
  • Ethanol / therapeutic use*
  • Female
  • Genetic Diseases, Inborn / pathology
  • Genetic Diseases, Inborn / physiopathology*
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Myoclonus / complications*
  • Myoclonus / genetics
  • Myoclonus / physiopathology
  • Tomography, X-Ray Computed

Substances

  • Ethanol