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Myoclonic Status in Non-Progressive Encephalopathies (MSNE) is a rare and intriguing epilepsy syndrome characterized by the early onset of continuous diffuse epileptiform abnormalities, concomitant myoclonic phenomena, and transient cognitive, motor, or behavioral disturbances [1]. This syndrome’s etiology encompasses three distinct categories: hereditary, structural brain malformations, and perinatal anoxic injury [2]. The following report details a case of MSNE associated with a mutation in the GRIN2A gene.