Amyotrophy in Shy-Drager syndrome

Acta Neurol Belg. 1983 May-Jul;83(3):142-57.

Abstract

Five cases of Shy-Drager Syndrome (SDS) are reported. All patients showed marked muscular wasting often with fasciculation and without sensory loss. Clinical, electromyographic and in one case, pathological findings in the spinal cord indicated a lesion at the level of the anterior born cell. An extensive review of the literature disclosed a significant number of cases of SDS displaying amyotrophy referable to a spinal lesions.

Publication types

  • Case Reports

MeSH terms

  • Autonomic Nervous System Diseases / complications*
  • Electromyography
  • Female
  • Humans
  • Male
  • Middle Aged
  • Muscles / pathology*
  • Muscular Atrophy / diagnosis
  • Muscular Atrophy / etiology*
  • Neural Conduction
  • Shy-Drager Syndrome / complications*
  • Shy-Drager Syndrome / pathology
  • Spinal Cord / pathology*