Familial infantile myoclonic epilepsy

A rare, genetic, infantile epilepsy syndrome disease characterized by neonatal- to infancy-onset myoclonic focal seizures occurring in various members of a family, associated in some with mild dysarthria, ataxia and borderline-to-moderate intellectual disability.

Also known as: FIME, familial infantile myoclonus epilepsy, myoclonic epilepsy, infantile, familial, Eim, myoclonic epilepsy, familial infantile

7 clinical trials for this condition and its sub-types, 0 tagged with Familial infantile myoclonic epilepsy itself.