Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle

J Neurol Sci. 1992 May;109(1):1-10. doi: 10.1016/0022-510x(92)90086-z.

Abstract

A sporadic case (female, aged 14 years) is reported who was affected by myopathy, restrictive cardiomyopathy and sensory motor polyneuropathy. A muscle biopsy showed accumulation of osmiophilic granular and filamentous material on electron microscopy, which stained positively in immunofluorescence for desmin. Increased desmin phosphorylated isoforms have been demonstrated by one- and two-dimensional electrophoresis. Sural nerve biopsy showed a peripheral neuropathy with giant axons, filled with closely packed neurofilaments. Clinical and morphological aspects of this new disease entity are discussed with regards to the classical form of giant axonal neuropathy and to other conditions of peripheral neuropathy with giant axons.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adolescent
  • Axons / ultrastructure*
  • Cardiomyopathy, Hypertrophic / genetics*
  • Cardiomyopathy, Hypertrophic / metabolism
  • Cardiomyopathy, Hypertrophic / pathology
  • Desmin / metabolism*
  • Desmin / ultrastructure
  • Diagnosis, Differential
  • Female
  • Genes, Recessive
  • Hereditary Sensory and Motor Neuropathy / diagnosis
  • Hereditary Sensory and Motor Neuropathy / genetics*
  • Hereditary Sensory and Motor Neuropathy / metabolism
  • Hereditary Sensory and Motor Neuropathy / pathology
  • Humans
  • Intermediate Filaments / ultrastructure*
  • Muscle Proteins / analysis
  • Muscles / pathology
  • Neuromuscular Diseases / genetics*
  • Neuromuscular Diseases / metabolism
  • Neuromuscular Diseases / pathology
  • Sural Nerve / pathology

Substances

  • Desmin
  • Muscle Proteins

Grants and funding