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Dravet's syndrome: Difference between revisions
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Revision as of 18:56, 30 June 2016
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] [2]
Links
- ↑ http://www.neurowikia.es/content/s%C3%ADndromes-epil%C3%A9pticos-de-la-primera-infancia
- ↑ Singh et al. 2001Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+? Epilepsia 42:837-844