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Dravet syndrome

Severe myoclonic epilepsy in infancyPolymorphic epilepsy in infancyPMEIEpilepsy with polymorphic seizures
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Type of Disease: Rare Condition or Disease Genetic, autosomal dominant Pediatric onset

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Genetic & Rare Diseases Information Center (GARD) GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish.

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DSF Website
Added On: Apr 21, 2015
Category: General
DSF's website provides information for caregivers and professional on the diagnosis, management and treatment of Dravet syndrome.