self-limited familial neonatal epilepsy
Findings
No curated finding names self-limited familial neonatal epilepsy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A neonatal/infantile epilepsy syndrome that is characterized by the onset of seizures that start in the in the neonate between day 1 and 7 of life and are often unilateral clonic events that recur and may alternate sides from seizure to seizure. Seizures can be repetitive over hours to days. Seizures remit by 4-6 months of age. A proportion of those affected may have seizures in later life. The child is expected to have typical developmental progress.
Definition from the Mondo Disease Ontology (MONDO:0100023), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- KCNQ3HGNC:6297
- Moderate · ClinGen · Autosomal dominant · 2023
Where it sits
- A kind of
Other names
1 name
Resolves to: self-limited familial neonatal epilepsy
- Also called
- self-limited familial and non-familial neonatal seizures