epilepsy with myoclonic absences
ep·i·lep·sy with my·o·clon·ic ab·senc·es
a form of generalized epilepsy characterized by absence seizures, severe bilateral rhythmic clonic jerks often associated with tonic contraction, and a 3-Hz spike and wave pattern found on an EEG. Age of onset is usually around 7 years and males are more often affected.
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