Familial infantile myoclonic epilepsy
Familial infantile myoclonic epilepsy
Definition
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 familial infantile myoclonus epilepsy, FIME, myoclonic epilepsy, infantile, familial — per MONDO