content:lennox-gastaut_syndrome

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 ====== Lennox-Gastaut syndrome ====== ====== Lennox-Gastaut syndrome ======
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 <alert type="warning" icon="glyphicon glyphicon-hand-down">This article is a stub. Please help us improve it</alert> <alert type="warning" icon="glyphicon glyphicon-hand-down">This article is a stub. Please help us improve it</alert>
 Lennox-Gastaut syndrome (LGS) is an epileptic encephalopathy and is defined by a triad of multiple drug-resistant seizure types, a specific EEG pattern showing bursts of slow spike-wave complexes or generalized paroxysmal fast activity, and intellectual disability. The prevalence of LGS is estimated between 1 and 2% of all patients with epilepsy.  Lennox-Gastaut syndrome (LGS) is an epileptic encephalopathy and is defined by a triad of multiple drug-resistant seizure types, a specific EEG pattern showing bursts of slow spike-wave complexes or generalized paroxysmal fast activity, and intellectual disability. The prevalence of LGS is estimated between 1 and 2% of all patients with epilepsy. 
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