“Familial Adult Myoclonus Epilepsy: A Slow-Progressing Neurodegenerative Disorder.”

https://pubmed.ncbi.nlm.nih.gov/38114875

Familial adult myoclonus epilepsy is a slow-progressing neurodegenerative disorder characterized by cortical myoclonic tremor, overt myoclonus, and rare bilateral tonic-clonic seizures, with diagnosis based on specific neurophysiological testing and imaging data indicating a cortical origin, and treatment mainly symptomatic.