Article
Clinical and Genetic Features of Dravet Syndrome: A Prime Example of the Role of Precision Medicine in Genetic Epilepsy
2023-11-28
Abstract excerpt
Dravet syndrome (DS), also known as severe myoclonic epilepsy of infancy, is a rare and drug-resistant form of developmental and epileptic encephalopathies, which is both debilitating and challenging to manage, typically arising during the first year of life, with seizures often triggered by fever, infections, or vaccinations. It is characterized by frequent and prolonged seizures, developmental delays, and variou...
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Identifiers and source
- Literature Corpus work
- e424365d-c324-5492-ab50-37417f94310f
- DOI
- 10.20944/preprints202311.1719.v1