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self-limited familial infantile epilepsy - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

self-limited familial infantile epilepsy

MONDO:0100024

Also known as:SeLFIEself-limited familial and non-familial infantile seizures

Overview

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.

Diagnosis

Biomarker and diagnostic research for self-limited familial infantile epilepsy has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for self-limited familial infantile epilepsy.

69 publications have been identified in PubMed for self-limited familial infantile epilepsy. Kisho has analyzed 51 by research type. Research spans Epidemiology / Natural History (31%), Review / Meta-Analysis (25%), and Clinical Trial Publication (12%).

Research Type	Count	% of Total
Disease patterns and progression	16	31%

Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 12:36 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

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self-limited familial infantile epilepsy

Overview

Diagnosis

Research Landscape

Medical References

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Questions for Your Care Team

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