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infant epilepsy with migrant focal crisis - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

infant epilepsy with migrant focal crisis

MONDO:0016026

Overview

An infantile epilepsy syndrome characterized by early-onset progressive encephalopathy with migrant, continuous myoclonus. Three cases have been reported. The focal continuous myoclonus appeared during the first months of life. Prolonged bilateral myoclonic seizures and generalized tonic-clonic seizures occurred later. Subsequently, a progressive encephalopathy with hypotonia and ataxia appeared. Cortical atrophy was revealed by computed tomography (CT) scan and magnetic resonance imaging (MRI). The etiology is unknown.

ResearchLimited published research (1 article)

Prognosis

Estimated prevalence: <1 in 1,000,000 (VERY_RARE).

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 infant epilepsy with migrant focal crisis.

1 publication has been identified in PubMed for infant epilepsy with migrant focal crisis. Research spans Case Report / Case Series (100%).

Recent Publications

Gebien DJ (2024). [PMID: 39451647](https://pubmed.ncbi.nlm.nih.gov/39451647/). *Diagnostics (Basel, Switzerland)*. [Case Report / Case Series]

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 9:58 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:1943

GARD

Genetic and Rare Diseases Info Center

GARD:2995

Questions for Your Care Team

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infant epilepsy with migrant focal crisis

Overview

Prognosis

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team