A Novo SCN1A Mutation Identified in a Chinese Family with Dravet Syndrome: A Case Study
Dravet syndrome (DS), also known as severe myoclonic epilepsy of infancy (SMEI), is one of the rare early childhood intractable epileptic encephalopathies associated with pleomorphic seizure activity, cognitive decline, motor, and behavioral abnormalities. The convulsive seizure is the most common type seen in DS [1]. After the first episode of seizure-like activity, be- havioral disorders […]
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