vitalwiki

Myoclonic epilepsy in non-progressive encephalopathies

ORPHA:86913· ICD-10 G40.4

Definition

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.

Prevalence
Unknown
Age of onset
Childhood, Infancy