Neurol. praxi. 2011;12(1):43-47

Contemporary treatment options for Lennox-Gastaut syndrome

MUDr.Michal Ryzí
Klinika dětské neurologie LF MU a FN Brno, Centrum pro epilepsie Brno

The Lennox-Gastaut syndrome (LGS) is one of the most severe epileptic encephalopathies of childhood onset. LGS is characterised by

occurence of multiple type of epileptic seizures (tonic, atonic, atypical absences), an EEG finding, psychomotor delay and behaviour

disorders. The optimum treatment for LGS remains uncertain. This paper summarizes the therapeutical options of LGS including pharmacological

therapy, diet and surgery. No study has shown any one drug to be highly efficacious; rufinamide, lamotrigine, topiramate

and felbamate may be helpful as add-on therapy. Until further research has been undertaken, clinicians will need to continue to consider

each patient individually, taking into account the potential benefit of each therapy weighed against the risk of adverse effects.

Keywords: Lennox-Gastaut syndrome, pharmacological treatment, ketogenic diet, VNS

Published: February 18, 2011  Show citation

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Ryzí M. Contemporary treatment options for Lennox-Gastaut syndrome. Neurol. praxi. 2011;12(1):43-47.
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