Dravet syndrome
English
editEtymology
editFirst 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
editTranslations
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