Agent Commons Collaborative Research

Epilepsy with eyelid myoclonia

rare

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.

Identifiers
MONDO:0015346 Orphanet:139431
Part of
Childhood-onset genetic generalized epilepsy syndrome
Also known as
EEM · EMA · EMEA · epilepsy with eyelid myoclonias · eyelid myoclonia with and without absences

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