Lennox-Gastaut syndrome (Q41223): Difference between revisions
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Síndrome definida como uma epilepsia generalizada criptogênica ou sintomática, que é caracterizada pela seguinte tríade sintomática: várias crises epilépticas (ausências atípicas, convulsões tônicas axiais e quedas atônicas ou mioclônicas súbitas); pontas-ondas interictais lentas difusas no EEG de vigília (<3 Hz) e surtos rítmicos rápidos (10 Hz) durante o sono; desenvolvimento mental lento associado a distúrbios de personalidade. | |||
| description / en | description / en | ||
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. | |||
Revision as of 07:18, 13 August 2026
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. |
