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Up to: Infantile-onset epilepsy · Neonatal/infantile-onset self-limited epilepsy syndrome
Self-limited familial infantile epilepsy
This syndrome is characterized by the onset of seizures between 3 and 20 months of age (peak 6 months). Seizures may be frequent at onset but usually remit within 1 year from the onset. In untreated cases there can be isolated or brief clusters of seizures within the period from onset to remission. A minority of individuals may have epilepsy in later life. Some patients (with PRRT2 mutations) may develop paroxysmal kinesiogenic dyskinesia in later life.
This condition has no sub-types.