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Up to: Developmental and epileptic encephalopathy · Neonatal/infantile-onset epilepsy syndrome with developmental and epileptic encephalopathy
Early-infantile DEE
A neonatal/infantile epilepsy syndrome characterized by frequent drug-resistant seizures that begin ≤3 months of age, with abnormal interictal EEG and neurological examination. In up to 80% of patients, EIDEE is caused by an underlying structural, genetic, or metabolic reason.