Epilepsy with eyelid myoclonia

A rare, idiopathic, generalized form of reflex epilepsy characterized by childhood onset, unique seizure manifestations, striking light sensitivity, and possible occurrence of generalized tonic-clonic seizures.

Also known as: EEM, EMA, EMEA, Epilepsy with Eyelid Myoclonia, Jeavons syndrome, epilepsy with eyelid myoclonias, eyelid myoclonia with and without absences

8 clinical trials for this condition and its sub-types.