Inclusion body myopathy-like changes in a family with cerebellar atrophy, mental retardation and abnormal pupils

Eur Neurol. 2006;56(3):172-4. doi: 10.1159/000096182. Epub 2006 Oct 11.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Biopsy
  • Electromyography
  • Family
  • Fathers
  • Female
  • Humans
  • Intellectual Disability / genetics
  • Intellectual Disability / pathology*
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Muscle, Skeletal / pathology
  • Myoclonic Cerebellar Dyssynergia / genetics
  • Myoclonic Cerebellar Dyssynergia / pathology*
  • Parents
  • Pupil Disorders / genetics
  • Pupil Disorders / pathology*