White-matter disease in 18q deletion (18q-) syndrome: magnetic resonance spectroscopy indicates demyelination or increased myelin turnover rather than dysmyelination

Neuroradiology. 2005 Jan;47(1):83-6. doi: 10.1007/s00234-004-1309-9. Epub 2005 Jan 11.

Abstract

Proton magnetic resonance spectroscopic data ((1)H-MR spectroscopy) of patients with 18q deletion syndrome have not yet been reported. (1)H-MR spectroscopy, performed in an affected 2-year-old girl with markedly delayed neuromotor development and typical supratentorial white-matter disease (WMD), showed an increase of choline and alpha-glutamate concentrations. Eight months later, simultaneously with clinical improvement, alpha-glutamate had normalised whereas choline remained slightly increased. Active demyelination or increased myelin turnover might contribute to the hitherto unexplained WMD of this rare disorder.

Publication types

  • Case Reports

MeSH terms

  • Aspartic Acid / analogs & derivatives*
  • Aspartic Acid / analysis
  • Brain Diseases / metabolism*
  • Choline / analysis
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 18 / genetics*
  • Demyelinating Diseases / diagnosis*
  • Female
  • Follow-Up Studies
  • Glutamic Acid / analysis
  • Humans
  • Infant
  • Inositol / analysis
  • Magnetic Resonance Imaging
  • Magnetic Resonance Spectroscopy*
  • Myelin Sheath / metabolism*

Substances

  • Aspartic Acid
  • Glutamic Acid
  • Inositol
  • N-acetylaspartate
  • Choline