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Epilepsia ; 52(1): 175-8, 2011 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-21219303

RESUMEN

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.


Asunto(s)
Epilepsias Mioclónicas/epidemiología , Convulsiones/epidemiología , Vacunación/efectos adversos , Adolescente , Niño , Preescolar , Vacuna contra Difteria, Tétanos y Tos Ferina/efectos adversos , Epilepsias Mioclónicas/complicaciones , Epilepsias Mioclónicas/genética , Humanos , Incidencia , Lactante , Mutación/genética , Canal de Sodio Activado por Voltaje NAV1.1 , Proteínas del Tejido Nervioso/genética , Estudios Retrospectivos , Convulsiones/etiología , Convulsiones/genética , Canales de Sodio/genética , Síndrome , Adulto Joven
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