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Up to: Hereditary neurological disease · Myoclonic epilepsy · Monogenic epilepsy
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.
This condition has no sub-types.