Myoclonic epilepsy in non-progressive encephalopathies

MONDO:0019488

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.

Also known as: myoclonic status in non-progressive encephalopathies, myoclonus epilepsy in non-progressive encephalopathies

7 clinical trials for this condition and its sub-types, 0 tagged with Myoclonic epilepsy in non-progressive encephalopathies itself.

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