Late-onset Lennox-Gastaut syndrome: Diagnostic evaluation and outcome

Conclusions Late-onset LGS represents a rare, treatment-resistant generalized epilepsy that is disabling and may be associated with progressive cognitive impairment. The elevated CSF protein level in our cohort could have been due to high seizure burden but increases the possibility of an inflammatory component to the pathophysiology of this disorder.
Source: Neurology Clinical Practice - Category: Neurology Authors: Tags: EEG, Generalized seizures Research Source Type: research