EEG features of glut-1 deficiency syndrome

Epilepsia. 2002 Aug;43(8):941-5. doi: 10.1046/j.1528-1157.2002.50401.x.

Abstract

Purpose: Glut-1 deficiency syndrome (Glut-1 DS) is caused by the deficiency of the major glucose transporter in cerebral microvessels.

Methods: We performed pre- and postprandial EEG recordings in two unrelated children with Glut-1 DS with developmental delay and seizures predominantly in the morning before breakfast.

Results: Extensive epileptiform discharges observed in the fasting state were improved markedly by food intake, as documented in EEG recordings 1 and 2 h after a meal. The ratio of cerebrospinal fluid glucose to blood glucose was decreased in both children. Glut-1 deficiency was confirmed by biochemical and molecular genetic investigations.

Conclusions: Pre- and postprandial EEG recordings offer a simple screening test for Glut-1 DS.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Blood Glucose / analysis
  • Child, Preschool
  • Electroencephalography*
  • Fasting / physiology
  • Female
  • Glucose / cerebrospinal fluid
  • Glucose Transporter Type 1
  • Humans
  • Male
  • Metabolism, Inborn Errors / physiopathology*
  • Monosaccharide Transport Proteins / deficiency*
  • Postprandial Period / physiology
  • Syndrome

Substances

  • Blood Glucose
  • Glucose Transporter Type 1
  • Monosaccharide Transport Proteins
  • SLC2A1 protein, human
  • Glucose