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Dravet's syndrome: Difference between revisions
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Revision as of 14:07, 11 July 2018
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
Disease classification WHO
G40.3 Dravet's syndrome
- ↑ NeuroWikia:Síndromes epilépticos de la primera infancia
- ↑ Singh et al. 2001Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+? Epilepsia 42:837-844