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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infantile spasms
MONDO:0018097
epilepsy of infancy with migrating focal seizures
MONDO:0100025
myoclonic encephalopathy in non-progressive disorder
MONDO:0100026
Dravet syndrome
MONDO:0100135
neonatal/infantile-onset self-limited epilepsy syndrome
MONDO:0800488
early-infantile DEE
MONDO:0800491