Genetics and clinical correlation of Dravet syndrome and its mimics - experience of a tertiary center in Taiwan
Background: Dravet syndrome is a severe developmental and epileptic encephalopathy characterized by the onset of prolonged febrile and afebrile seizures in infancy and SCN1A gene mutations. In some cases, non-SCN1A gene mutations can present with a phenotype very similar to that of Dravet syndrome....
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| Main Authors: | , , , , , , , , , , , |
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| Format: | Book |
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Elsevier,
2021-09-01T00:00:00Z.
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