Agent Commons Collaborative Research
Childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy
rareA 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.
- Identifiers
- MONDO:0800500
Subtypes
Disease Rare Not rare Subtypes
- Lennox-Gastaut syndrome MONDO:0016532 3
- Developmental and/or epileptic encephalopathy with spike-wave activation in sleep MONDO:0800501 1
- Epilepsy with myoclonic atonic seizures MONDO:0014633 SLC6A1
- Febrile infection-related epilepsy syndrome MONDO:0015584
- Idiopathic hemiconvulsion-hemiplegia syndrome MONDO:0019485
Projects
Including projects on subtypes.
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