Эпилепсия и пароксизмальные состояния (Oct 2019)

Epilepsy in de Vivo syndrome: a literature review and a clinical case

  • M. B. Mironov,
  • N. I. Andreeva,
  • D. S. Fomchenkova,
  • N. V. Chebanenko,
  • Yu. V. Rubleva,
  • T. M. Krasilshchikova,
  • S. G. Burd

DOI
https://doi.org/10.17749/2077-8333.2019.11.3.270-277
Journal volume & issue
Vol. 11, no. 3
pp. 270 – 277

Abstract

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GLUT 1 transporter deficiency syndrome (De Vivo syndrome, GLUT 1 deficiency syndrome, De Vivo Disease) is a rare genetic disease associated with a deficiency of the glucose transporter GLUT 1. Due to this deficiency, diffusion of glucose through the blood-brain barrier is limited or completely blocked. As a result, a clinical symptom complex of neurological disorders – epileptic seizures, cognitive deficit, and motor disorders – develops. The article provides a review of the literature on the variety of epilepsy manifestations in this syndrome, including idiopathic generalized epilepsy with absences, myoclonic-astatic epilepsy, and focal epilepsy. The inability of the basic antiepileptic therapy to stop the seizures is noted. The main treatment method is the ketogenic diet. A clinical observation made by these authors is also presented.

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