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Up to: Neonatal/infantile epilepsy syndrome
Neonatal/infantile-onset epilepsy syndrome with developmental and epileptic encephalopathy
A neonatal/infantile epilepsy syndrome characterized by the onset of non-self-limiting seizures and developmental regression or delay in infants/neonates. This condition is typically caused by genetic mutations that disrupt normal brain development, affecting both cognitive and motor development that is not responsive to typical seizure treatments.
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Dravet syndrome 39 trials
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Infantile spasms 8 trials · 19 incl. sub-types Sub-types →
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Early-infantile DEE 2 trials Sub-types →