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Dravet's syndrome: Difference between revisions
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[[epilepsy|Generalized epilepsy with febrile seizures plus]] | [[epilepsy|Generalized epilepsy with febrile seizures plus]] | ||
Dravet syndrome corresponds a phenotype severe myoclonic epilepsy of infancy (SMEI).<ref>http://www.neurowikia.es/content/s%C3%ADndromes-epil%C3%A9pticos-de-la-primera-infancia</ref><references/> | '''Dravet syndrome''' corresponds a phenotype severe myoclonic epilepsy of infancy (SMEI), a form of intractable epilepsy of childhood.<ref>http://www.neurowikia.es/content/s%C3%ADndromes-epil%C3%A9pticos-de-la-primera-infancia</ref> | ||
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Revision as of 22:30, 25 July 2015
Generalized epilepsy with febrile seizures plus Dravet syndrome corresponds a phenotype severe myoclonic epilepsy of infancy (SMEI), a form of intractable epilepsy of childhood.[1]