Childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy

MONDO:0800500

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.

45 clinical trials for this condition and its sub-types, 0 tagged with Childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy itself.

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↑ Childhood-onset epilepsy syndrome (106)

Sub-types of Childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy

Lennox-Gastaut syndrome 26 trials · 27 incl. sub-types
3 sub-types
- Developmental and epileptic encephalopathy 94 1 trial
- Developmental and epileptic encephalopathy, 31A 0 trials
- Developmental and epileptic encephalopathy, 43 0 trials
Developmental and/or epileptic encephalopathy with spike-wave activation in sleep 8 trials
1 sub-type
- GRIN2A-related developmental and/or epileptic encephalopathy with spike-wave activation in sleep 0 trials
Epilepsy with myoclonic atonic seizures 1 trial
Febrile infection-related epilepsy syndrome 1 trial
Idiopathic hemiconvulsion-hemiplegia syndrome 0 trials

Including sub-types (45) Tagged with Childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy (0)

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