Abnormality of cerebral gangliosides in Fukuyama type congenital muscular dystrophy

Brain Dev. 1995 Jan-Feb;17(1):33-7. doi: 10.1016/0387-7604(94)00114-d.

Abstract

Compared with DMD cases and non-neuromuscular disease controls, FCMD cases showed a reduction of total gangliosides, and an abnormal, immature ganglioside pattern in the cerebral gray and white matter. However, GM4, which is only found in myelin and oligodendroglia, and is a unique quantitative marker of myelination, was present in a relatively high percentage in the white matter, which showed frontal lobe micropolygyria and diffuse low density on CT and MR T1-imaging.

MeSH terms

  • Adolescent
  • Adult
  • Biomarkers
  • Brain / pathology*
  • Brain Chemistry*
  • Cerebral Cortex / chemistry
  • Child, Preschool
  • Female
  • Fetus / pathology
  • Frontal Lobe / chemistry
  • G(M1) Ganglioside / metabolism
  • Gangliosides / metabolism*
  • Humans
  • Infant, Newborn
  • Male
  • Muscular Dystrophies / congenital
  • Muscular Dystrophies / metabolism
  • Muscular Dystrophies / pathology*

Substances

  • Biomarkers
  • Gangliosides
  • G(M1) Ganglioside
  • ganglioside, GM4