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benign familial infantile convulsions
Genetics:
- defects in SCN2A associated with type 3 (autosomal dominant)
Clinical manifestations:
- afebrile seizures occur in clusters during the 1st year of life, without neurologic sequelae (type 3)
Differential diagnosis:
- distinguished from benign neonatal epilepsy by a later age at onset
Related
benign familial neonatal epilepsy
General
epilepsy
Database Correlations
OMIM 607745
References
OMIM :accession 607745