Early-infantile DEE
Early-infantile DEE
Definition
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.
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, EIDEE, EIEE, EME, epileptic encephalopathy, early infantile, epileptic encephalopathy, infantile, infantile epileptic encephalopathy, Ohtahara syndrome — per MONDO
Also identified as
- DOID 0050709 per MONDO
- DOID 2481 per MONDO
- DOID 308 per MONDO
- ICD9 345.6 per MONDO
- NCIT C116593 per MONDO
- Orphanet 1934 per MONDO
- Orphanet 1935 per MONDO
- SCTID 230429005 per MONDO
- SCTID 44423001 per MONDO
- UMLS C0393706 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Brain | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Brain | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Central nervous system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Central nervous system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Nervous system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Nervous system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |