Transition for patients with epilepsy due to metabolic and mitochondrial disorders

Eric H. Kossoff, Pierangelo Veggiotti, Pierre Genton, Isabelle Desguerre

Research output: Contribution to journalArticle


The transition of adolescents with refractory epilepsy to the care of adult neurologists can be challenging. For those patients with epilepsy due to mitochondrial disorders, Lafora disease, Unverricht-Lundborg disease, and GLUT1 deficiency syndrome, a successful transition can be even more problematic for both caregivers and neurologists. Many of these patients require dietary treatments (ketogenic and modified Atkins diets) for long-term management of their epilepsy. For these patients, coordinating transfer of their dietary management is necessary.

Original languageEnglish (US)
Pages (from-to)37-40
Number of pages4
Issue numbers3
StatePublished - Aug 1 2014


  • GLUT1
  • Ketogenic
  • Ketosis
  • Lafora
  • Mitochondria
  • Unverricht-Lundborg

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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