Pediatric Neurology
Volume 37, Issue 2 , Pages 130-133, August 2007

GLUT1 Deficiency With Delayed Myelination Responding to Ketogenic Diet

  • Jörg Klepper, MD

      Affiliations

    • Children’s Hospital Aschaffenburg, Aschaffenburg; Germany
    • Corresponding Author InformationCommunications should be addressed to: Dr. Klepper; Children’s Hospital Aschaffenburg; Am Hasenkopf; D-63739 Aschaffenburg; Germany.
  • ,
  • Volkher Engelbrecht, MD

      Affiliations

    • Department of Radiology, Klinikum St. Marien, Amberg, Germany
  • ,
  • Hans Scheffer, PhD

      Affiliations

    • Department of Human Genetics, University Medical Center Nijmegen, The Netherlands
  • ,
  • Marjo S. van der Knaap, MD, PhD

      Affiliations

    • Department of Child Neurology, VU University Medical Center, Amsterdam, The Netherlands.
  • ,
  • Andreas Fiedler, MD

      Affiliations

    • Department of Pediatrics, Klinikum St. Marien, Amberg, Germany

Received 23 October 2006; accepted 22 March 2007.

Monitoring effects of a ketogenic diet in GLUT1 deficiency syndrome without seizures is difficult. Neuroimaging is considered uninformative. We report the case of a boy with neurodevelopmental delay, severe ataxia, an E54X-mutation in the SLC2A1 gene (previously GLUT1), and neuroimaging abnormalities indicative of delayed myelination. Six months on a ketogenic diet resulted in an improved high subcortical white matter signal on T2-weighted images and a reduced N-acetylaspartate/creatine ratio. We conclude that delayed subcortical myelination may occur in GLUT1 deficiency syndrome as a nonspecific finding reflecting developmental delay. In patients without seizures, cranial magnetic resonance imaging and magnetic resonance spectroscopy may prove useful tools to monitor the response to a ketogenic diet.

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PII: S0887-8994(07)00130-0

doi:10.1016/j.pediatrneurol.2007.03.009

Pediatric Neurology
Volume 37, Issue 2 , Pages 130-133, August 2007