Proton magnetic resonance spectroscopy and diffusion-weighted imaging in isolated sulfite oxidase deficiency

J Child Neurol. 2006 Sep;21(9):801-5. doi: 10.1177/08830738060210090601.

Abstract

Isolated sulfite oxidase deficiency is a rare autosomal recessive disorder of the newborn that can be mistaken for neonatal asphyxia. Diffusion-weighted imaging of the brain demonstrates widespread diffusion restriction, and proton magnetic resonance spectroscopy shows an elevated lactate level, a decrease in the ratio of N-acetylaspartate to creatine, and a rise in the ratio of choline to creatine. This precedes severe cystic encephalomalacia and suggests that the energy failure associated with neuronal dysfunction and myelin disintegration occurs early in isolated sulfite oxidase deficiency.

Publication types

  • Case Reports

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / complications
  • Amino Acid Metabolism, Inborn Errors / diagnosis*
  • Amino Acid Metabolism, Inborn Errors / enzymology
  • Amino Acid Metabolism, Inborn Errors / genetics
  • Brain Diseases, Metabolic, Inborn / complications
  • Brain Diseases, Metabolic, Inborn / diagnosis*
  • Brain Diseases, Metabolic, Inborn / enzymology
  • Brain Diseases, Metabolic, Inborn / genetics
  • Diagnosis, Differential
  • Diffusion Magnetic Resonance Imaging
  • Electroencephalography
  • Gene Deletion
  • Humans
  • Hypoxia-Ischemia, Brain / diagnosis
  • Infant
  • Infant, Newborn
  • Magnetic Resonance Spectroscopy
  • Male
  • Seizures / enzymology
  • Seizures / etiology
  • Sulfite Oxidase / deficiency*
  • Sulfite Oxidase / genetics

Substances

  • Sulfite Oxidase