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generalized epilepsy & paroxysmal dyskinesia
Genetics:
- associated with defects in KCNMA1
Clinical manifestations:
- coexistence of epilepsy & paroxysmal dyskinesia
- absence seizures
- generalized tonic-clonic seizures
- paroxysmal nonkinesigenic dyskinesia
- involuntary dystonic or choreiform movements
- onset is usually in childhood
- patients may have seizures only, dyskinesia only, or both
General
genetic syndrome (multisystem disorder)
epilepsy
paroxysmal dyskinesia
Database Correlations
OMIM 609446
References
OMIM :accession 609446