Central nervous system malformations in ethylmalonic encephalopathy

Am J Med Genet. 1998 Jan 23;75(3):292-6.

Abstract

Central nervous system malformations have been reported in a number of inherited enzyme defects. Ethylmalonic encephalopathy, an organic aciduria of unknown pathogenesis, has not been reported previously in association with brain or spinal cord malformations. We report on 2 sibs with confirmed ethylmalonic encephalopathy and malformations of the central nervous system; one with tethered cord, the other with cerebellar tonsillar ectopia (Chiari I malformation).

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Brain / abnormalities*
  • Child, Preschool
  • Female
  • Growth Disorders / genetics
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Malonates / urine*
  • Metabolism, Inborn Errors / genetics*
  • Spine / abnormalities*
  • Succinates / urine

Substances

  • Malonates
  • Succinates
  • ethylmalonic acid
  • methylsuccinic acid