Wikisage, the free encyclopedia of the second generation, is digital heritage
Dravet's syndrome: Difference between revisions
Jump to navigation
Jump to search
mNo edit summary |
mNo edit summary |
||
| Line 1: | Line 1: | ||
[[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), 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 NeuroWikia:Síndromes epilépticos 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> | ||
==Links== | ==Links== | ||
Revision as of 02:45, 1 July 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
- ↑ NeuroWikia:Síndromes epilépticos de la primera infancia
- ↑ Singh et al. 2001Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+? Epilepsia 42:837-844