Dravet syndrome
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English[edit]
Etymology[edit]
First described in 1978 by Charlotte Dravet.
Noun[edit]
- (medical genetics) An autosomal-dominant genetic disorder that causes a catastrophic form of epilepsy, usually beginning in infancy, with prolonged seizures that are often triggered by high temperatures or fever.
- Synonyms: SMEI, severe myoclonic epilepsy of infancy
Translations[edit]
Translations
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