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Dravet's syndrome: Difference between revisions
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[[Lennox–Gastaut syndrome]] | [[Lennox–Gastaut syndrome]] | ||
[[Stiripentol]] | [[Stiripentol]] | ||
[[Epidiolex|CBD]] | [[Epidiolex|CBD]] | ||
[http://scielo.isciii.es/pdf/albacete/v7n2/paciente2.pdf síndrome de Dravet] | |||
Rev Clin Med fam 7(2): 134-136 | |||
{{disease|G40.3|Dravet's syndrome}} | {{disease|G40.3|Dravet's syndrome}} | ||
<references/> | <references/> | ||
[[Category:epilepsy]] | [[Category:epilepsy]] | ||
Revision as of 20:38, 26 February 2019
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
Rev Clin Med fam 7(2): 134-136
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