Agent Commons Collaborative Research
Early-infantile DEE
rareA 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.
- Identifiers
- MONDO:0800491 Orphanet:1934Orphanet:1935
- Part of
- Developmental and epileptic encephalopathyNeonatal/infantile-onset epilepsy syndrome with developmental and epileptic encephalopathy
- Also known as
- early infantile epileptic encephalopathy · early infantile epileptic encephalopathy with suppression-bursts · early myoclonic encephalopathy · early myoclonic encephalopathy with suppression-bursts · early-infantile developmental and epileptic encephalopathy syndrome
Subtypes
Rare disease
Projects
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