self-limited familial infantile epilepsy
Findings
No curated finding names self-limited familial infantile epilepsy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0100024), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
2 names
Resolves to: self-limited familial infantile epilepsy
- Also called
- self-limited familial and non-familial infantile seizuresSeLFIE