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8A62.1 Lennox-Gastaut syndrome

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Syndrome defined as a cryptogenic or symptomatic generalised epilepsy, which is characterised by the following symptomatic triad: several epileptic seizures (atypical absences, axial tonic seizures and sudden atonic or myoclonic falls); diffuse slow interictal spike waves in the waking EEG (< 3 Hz) and fast rhythmic bursts (10 Hz) during sleep; slow mental development associated with personality disturbances.

synonyms

• Lennox-Gastaut syndrome

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