Fifty year follow-up of a patient with central core disease shows slow but definite progression

Neuromuscul Disord. 1998 Aug;8(6):385-91. doi: 10.1016/s0960-8966(98)00043-1.

Abstract

The follow-up of a patient with central core disease (CCD) over 50 years showed that although initially the condition was moderately non-progressive, progression of a significant degree did eventually occur. Histopathological and electron microscopic data were available from muscle biopsies carried out at the ages of 19 and 55 years, and show a marked predominance of type 1 fibres with central cores in most fibres at both ages. The four mutations within the RYR1 gene described in association with CCD and three of the more common malignant hyperthermia-associated mutations within RYR1 were not present.

Publication types

  • Case Reports

MeSH terms

  • DNA / genetics
  • Disease Progression
  • Follow-Up Studies
  • Humans
  • Male
  • Microscopy, Electron
  • Middle Aged
  • Muscle Fibers, Skeletal / pathology
  • Muscles / pathology
  • Mutation
  • Myopathies, Nemaline / genetics
  • Myopathies, Nemaline / pathology*
  • Myopathies, Nemaline / physiopathology*
  • Time Factors

Substances

  • DNA