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Child Neurology: Dravet syndrome: When to suspect the diagnosis
Dravet syndrome (DS), previously known as severe myoclonic epilepsy in infancy (SMEI), is an epileptic encephalopathy that presents with prolonged seizures in the first year of life. The seizures often occur with fever or illness, and are frequently initially categorized as febrile seizures. The cor...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Academy of Neurology
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2754329/ https://ncbi.nlm.nih.gov/pubmed/19786689 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e3181b9c880 |
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