Resumo

PEREZ, Ana Beatríz  e  MORENO, Nigeria. Dravet Syndrome. Salus [online]. 2015, vol.19, n.3, pp.27-30. ISSN 1316-7138.

Dravet syndrome (DS) is a severe epileptic encephalopathy that begins in the first year of life with crises usually triggered by fever which is followed by drug-resistant epilepsy. Also By Charlotte Dravet and recognize as an epilepsy syndrome by the International League against Epilepsy in 1985. For female preschool age 4, who starts tonic-clonic seizures from 6 months of age, presented with multiple convulsive seizures, cognitive and language delay, right hemiparesis EEG changes and drug resistance. Genetic study was performed with Novo alterations in gene SCN1A.

Palavras-chave : Seizures; Dravet syndrome; epilepsy.

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