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.

Also known as: SeLFIE, self-limited familial and non-familial infantile seizures

7 clinical trials for this condition and its sub-types, 0 tagged with Self-limited familial infantile epilepsy itself.