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Dravet's syndrome: Difference between revisions

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[[Epidiolex|CBD]]
[[Epidiolex|CBD]]


[https://linkinghub.elsevier.com/retrieve/pii/B978-0-444-52891-9.00065-8 DRAVET syndrome (severe myoclonic epilepsy in infancy)
Dravet, Charlotte & Hirokazu Oguni [https://linkinghub.elsevier.com/retrieve/pii/B978-0-444-52891-9.00065-8 DRAVET syndrome (severe myoclonic epilepsy in infancy)


[http://scielo.isciii.es/pdf/albacete/v7n2/paciente2.pdf síndrome de Dravet]
[http://scielo.isciii.es/pdf/albacete/v7n2/paciente2.pdf síndrome de Dravet]

Revision as of 20:42, 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

Lennox–Gastaut syndrome

Stiripentol

CBD

Dravet, Charlotte & Hirokazu Oguni [https://linkinghub.elsevier.com/retrieve/pii/B978-0-444-52891-9.00065-8 DRAVET syndrome (severe myoclonic epilepsy in infancy)

síndrome de Dravet

Rev Clin Med fam 7(2): 134-136

Disease classification WHO
G40.3 Dravet's syndrome