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.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Myoclonic epilepsy (16)

Including sub-types (7) Tagged with Myoclonic epilepsy in non-progressive encephalopathies (0)

Trials to join now! 4 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

Myoclonic epilepsy in non-progressive encephalopathies

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