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childhood absence epilepsy type 3
Genetics:
- associated with defects in CLCN2
Clinical manifestations:
1) onset at age 6-7 years
2) frequent absence seizures (several per day)
3) during adolescence, tonic-clonic & myoclonic seizures develop
Special laboratory:
- electroencephalogram
- bilateral, synchronous, symmetric 3 Hz spike waves
Related
epilepsy with grand mal seizures on awakening
juvenile absence epilepsy
General
childhood absence epilepsy
Database Correlations
OMIM 607682
References
UniProt :accession P51788