Epilepsy characterised by the occurrence of repeated seizures in healthy infants with no prior medical history during the first year of life. The seizures manifest with motor arrest, impairment of consciousness, staring, eye and head deviation, and mild unilateral clonic convulsions. A family history of the same epilepsy is a constant finding. The pattern of inheritance is most probably autosomal dominant.
Also indexed as
Benign familial infantile epilepsyBenign infantile focal epilepsy with midline spikes and waves during sleepICCA - [Infantile convulsions and choreoathetosis] syndromeInfantile convulsions and paroxysmal choreoathetosisInfantile convulsions or choreoathetosisWatanabe-Vigevano syndrome
Nearby in Genetic epileptic syndromes with onset in infancy