self-limited familial infantile epilepsy 2018-06-22T23:46:09Z https://github.com/monarch-initiative/mondo/issues/5740 https://github.com/monarch-initiative/mondo/issues/5792 https://github.com/monarch-initiative/mondo/issues/9285 GARD:0027273 SeLFIE self-limited familial and non-familial infantile seizures 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. MONDO:0100024 infantile-onset epilepsy neonatal/infantile-onset self-limited epilepsy syndrome