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Dravet's syndrome: Difference between revisions
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'''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> | '''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> | ||
<ref>Singh et al. 2001[http://onlinelibrary.wiley.com/doi/10.1046/j.1528-1157.2001.042007837.x/epdf Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?] Epilepsia 42:837-844</ref> | <ref>Singh et al. 2001[http://onlinelibrary.wiley.com/doi/10.1046/j.1528-1157.2001.042007837.x/epdf Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?] Epilepsia 42:837-844</ref> | ||
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[[Lennox–Gastaut syndrome]] | |||
<references/> | <references/> | ||
Revision as of 22:38, 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] [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