A new familial syndrome with dystonia and lower limb action myoclonus

Mov Disord. 2011 Apr;26(5):896-900. doi: 10.1002/mds.23557. Epub 2011 Mar 2.

Abstract

Background: Myoclonus-dystonia (M-D) is genetic and clinically heterogeneous. Identification and description of rare M-D syndromes may contribute to gene identification.

Results: Here, we describe a new, autosomal dominant M-D syndrome in a 3-generation pedigree showing anticipation. Patients have progressive action-induced multifocal dystonia and generalized myoclonus. A remarkable feature of the syndrome is action myoclonus in the lower extremities triggered by upright posture, causing instability. Electrophysiological characterization shows a 12-Hz peak in the EMG autospectrum and corticomuscular and intermuscular coherences.

Conclusions: A new familial M-D syndrome with progressive action myoclonus and dystonia is described.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged, 80 and over
  • Child
  • Dystonia / complications*
  • Dystonia / genetics*
  • Electroencephalography / methods
  • Electromyography
  • Family Health*
  • Female
  • Humans
  • Lower Extremity / physiopathology*
  • Magnetic Resonance Imaging / methods
  • Male
  • Middle Aged
  • Myoclonus / complications*
  • Myoclonus / genetics*
  • Sarcoglycans / genetics

Substances

  • Sarcoglycans