Lennox-Gastaut syndrome (Q41223): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed an Item |
||||||||||||||
| (7 intermediate revisions by the same user not shown) | |||||||||||||||
| description / pt-br | description / pt-br | ||||||||||||||
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. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/651135242 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:8A62.1 | |||||||||||||||
| Property / CURIE: CID11:8A62.1 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-8A62.1 | |||||||||||||||
| Property / Canary Token: dki-india-8A62.1 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Linked ICD 10 | |||||||||||||||
| Property / Linked ICD 10: G40.4 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest 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. |
Statements
CID11:8A62.1
0 references
dki-india-8A62.1
0 references
Concluído
0 references
13 August 2026
0 references
