A childhood-onset epilepsy syndrome where the onset of the condition includes manifestations of cognitive, neurological, or psychiatric impairment, stagnation, or regression, due directly to the underlying etiology. In contrast, an epileptic encephalopathy (EE) is present when the encephalopathy is caused by the epileptic activity. The term developmental and epileptic encephalopathy (DEE) is used when both factors contribute to the patient’s condition.
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self-limited childhood occipital epilepsy
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Landau-Kleffner syndrome
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rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
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epilepsy with myoclonic atonic seizures
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perioral myoclonia with absences
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febrile infection-related epilepsy syndrome
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