Epilepsy with eyelid myoclonia

MONDO:0015346

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, 0 tagged with Epilepsy with eyelid myoclonia itself.

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Where it sits in the disease tree

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Part of

↑ Childhood-onset genetic generalized epilepsy syndrome (0)

Including sub-types (8) Tagged with Epilepsy with eyelid myoclonia (0)

Trials to join now! 5 Not yet finished but already full! 2 Completed 1

Routine EEGs may hold hidden clues to childhood epilepsy — a new analysis method is put to the test

Diagnosis Completed

This study is testing whether a computer tool called BioEP can detect signs of seizure susceptibility in standard EEG recordings from children with epilepsy. Researchers will analyze past EEGs from 530 children aged 2 to 18 who already have an epilepsy diagnosis. The goal is to s…

Sponsor: Neuronostics Ltd • Aim: Diagnosis

Last updated Aug 01, 2026 00:00 UTC

Epilepsy with eyelid myoclonia

Where it sits in the disease tree

Routine EEGs may hold hidden clues to childhood epilepsy — a new analysis method is put to the test