Dravet syndrome (Q41208): Difference between revisions
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13 August 2026
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| Property / Linked ICD 10: G40.0 / rank | |||||||||||||||
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Latest revision as of 07:16, 13 August 2026
A refractory epileptic encephalopathy occurring in otherwise healthy infants during the first year of life with clonic/tonic-clonic, generalised and unilateral seizures, hemiclonic or generalised status epilepticus. The interictal EEG may initially be normal but with time background activity deteriorates and bilateral asymmetric, focal or multifocal paroxysms of polyspike and slow-waves appear. Mutations in the voltage-gated sodium channel gene SCN1A are commonly found.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A61.11 |
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| English | Dravet syndrome |
A refractory epileptic encephalopathy occurring in otherwise healthy infants during the first year of life with clonic/tonic-clonic, generalised and unilateral seizures, hemiclonic or generalised status epilepticus. The interictal EEG may initially be normal but with time background activity deteriorates and bilateral asymmetric, focal or multifocal paroxysms of polyspike and slow-waves appear. Mutations in the voltage-gated sodium channel gene SCN1A are commonly found. |
Statements
CID11:8A61.11
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dki-india-8A61.11
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Concluído
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13 August 2026
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