摘要Developmental and epileptic encephalopathies(DEEs)are neurological disorders generally involving medically intractable seizures and a diverse array of comorbid neuropsychiatric delays and deficits that may severely affect cognition,mood,sleep,social behavior,movement control,learning,and/or memory.Dravet syndrome(DS),also known as Severe Myoclonic Epilepsy of Infancy,is a rare disease but one of the more common DEEs,afflicting children in infancy and causing severe lifelong struggles and high risk of early mortality(Villas et al.,2017).
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