Lennox-Gastaut syndrome (Q41223)
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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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A62.1 |
||
| English | Lennox-Gastaut syndrome |
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. |
Statements
CID11:8A62.1
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dki-india-8A62.1
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Concluído
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13 August 2026
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