Paroxysmal events in glucose transporter type 1 deficiency syndrome: Early identification of their true nature is important

Dev Med Child Neurol. 2024 Nov;66(11):1403-1404. doi: 10.1111/dmcn.16000. Epub 2024 Jun 17.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Carbohydrate Metabolism, Inborn Errors* / diagnosis
  • Carbohydrate Metabolism, Inborn Errors* / genetics
  • Carbohydrate Metabolism, Inborn Errors* / physiopathology
  • Humans
  • Infant
  • Male
  • Monosaccharide Transport Proteins / deficiency
  • Monosaccharide Transport Proteins / genetics

Substances

  • Monosaccharide Transport Proteins

Supplementary concepts

  • Glut1 Deficiency Syndrome