Congenital neuromuscular disease with type I fibre hypotrophy, ophthalmoplegia and myofibril degeneration

J Neurol Neurosurg Psychiatry. 1982 Jun;45(6):507-12. doi: 10.1136/jnnp.45.6.507.

Abstract

We report a 7-year-old boy with progressive, early onset somatic and cranial muscle weakness associated with external ophthalmoplegia, facial weakness, type I fibre hypotrophy and myofibril degeneration. We separate this condition from congenital fibre type disproportion because of the facial weakness, ophthalmoplegia, central nucleation, and lysis in type I fibres. The case, which is similar to that described by Bender and Bender (1977), nosologically should be classified between the centronuclear myopathies and congenital fibre type disproportion, and most likely represents a congenital or neonatal disturbance of trophic interaction between nerve and muscle.

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Blepharoptosis / congenital
  • Blepharoptosis / pathology
  • Child
  • Humans
  • Male
  • Microscopy, Electron
  • Muscle Hypotonia / congenital
  • Muscle Hypotonia / pathology
  • Muscles / pathology*
  • Muscular Atrophy / congenital*
  • Muscular Atrophy / pathology
  • Myofibrils / pathology*
  • Neuromuscular Diseases / congenital*
  • Neuromuscular Diseases / pathology
  • Ophthalmoplegia / congenital*
  • Ophthalmoplegia / pathology