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Epilepsia ; 52(1): 175-8, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21219303

RESUMO

Dravet syndrome is a severe epileptic encephalopathy starting in the first year of life. Mutations in SCN1A can be identified in the majority of patients, and epileptic seizures in the setting of fever are a clinical hallmark. Fever is also commonly seen after vaccinations and provocation of epileptic seizures by vaccinations in patients with Dravet syndrome has been reported, but not systematically assessed. In a retrospective evaluation of 70 patients with Dravet syndrome and SCN1A mutations, seizures following vaccinations were reported in 27%. In 58% of these patients vaccination-related seizures represented the first clinical manifestation. The majority of seizures occurred after DPT vaccinations and within 72 h after vaccination. Two-thirds of events occurred in the context of fever. Our findings highlight seizures after vaccinations as a common feature in Dravet syndrome and emphasize the need for preventive measures for seizures triggered by vaccination or fever in these children.


Assuntos
Epilepsias Mioclônicas/epidemiologia , Convulsões/epidemiologia , Vacinação/efeitos adversos , Adolescente , Criança , Pré-Escolar , Vacina contra Difteria, Tétano e Coqueluche/efeitos adversos , Epilepsias Mioclônicas/complicações , Epilepsias Mioclônicas/genética , Humanos , Incidência , Lactente , Mutação/genética , Canal de Sódio Disparado por Voltagem NAV1.1 , Proteínas do Tecido Nervoso/genética , Estudos Retrospectivos , Convulsões/etiologia , Convulsões/genética , Canais de Sódio/genética , Síndrome , Adulto Jovem
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