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A rare epilepsy syndrome characterized by recurrent, long-lasting myoclonic status in infants and young children with a non-progressive encephalopathy, associated with transient and recurring motor, cognitive and/or behavioral disturbances.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for myoclonic epilepsy in non-progressive encephalopathies.
5 publications have been identified in PubMed for myoclonic epilepsy in non-progressive encephalopathies. Research spans Review / Meta-Analysis (40%), Case Report / Case Series (40%), and Basic Science / Preclinical (20%).
K Y M (2026). [PMID: 41579020](https://pubmed.ncbi.nlm.nih.gov/41579020/). *Epileptic Disord*. [Case Report / Case Series]
Magro G (2025). [PMID: 40869578](https://pubmed.ncbi.nlm.nih.gov/40869578/). *J Clin Med*. [Review / Meta-Analysis]
Kapoor D (2025). [PMID: 40794016](https://pubmed.ncbi.nlm.nih.gov/40794016/). *Epileptic Disord*. [Review / Meta-Analysis]
Hojo M (2024). [PMID: 39627236](https://pubmed.ncbi.nlm.nih.gov/39627236/). *Hum Genome Var*. [Case Report / Case Series]
van der Veen S (2024). [PMID: 39314082](https://pubmed.ncbi.nlm.nih.gov/39314082/). *Mov Disord*. [Basic Science / Preclinical]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 12:05 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center