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Up to: Childhood-onset epilepsy syndrome
Childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy
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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Lennox-Gastaut syndrome 26 trials · 27 incl. sub-types Sub-types →