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A disorder characterized onset at birth of profound encephalopathy with hypotonia, Respiratory insufficiency central hypoventilation, a persistent suppression burst pattern of EEG background, and recurrent bouts of myoclonus that are not accompanied by epileptic discharges on electroencephalography. Evolution to pharmacoresistant seizures is common and continued profound global developmental delay.
No clinical trials have been registered for neonatal encephalopathy with non-epileptic myoclonus.
4 publications have been identified in PubMed for neonatal encephalopathy with non-epileptic myoclonus. Research spans Case Report / Case Series (50%), Review / Meta-Analysis (25%), and Basic Science / Preclinical (25%).
Alammary D (2026). [PMID: 41573381](https://pubmed.ncbi.nlm.nih.gov/41573381/). *JIMD Rep*. [Case Report / Case Series]
Kapoor D (2025). [PMID: 40794016](https://pubmed.ncbi.nlm.nih.gov/40794016/). *Epileptic Disord*. [Review / Meta-Analysis]
Calligaris S (2024). [PMID: 39432297](https://pubmed.ncbi.nlm.nih.gov/39432297/). *Epileptic Disord*. [Case Report / Case Series]
Hojo M (2024). [PMID: 39627236](https://pubmed.ncbi.nlm.nih.gov/39627236/). *Hum Genome Var*. [Basic Science / Preclinical]
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 6:52 AM UTC