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Epilepsy, familial adult myoclonic

MONDO:0000160

An epilepsy syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities.

7 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, familial adult myoclonic itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary neurological disease (5791) ↑ Myoclonic epilepsy (16)

Sub-types of Epilepsy, familial adult myoclonic

Benign adult familial myoclonic epilepsy 0 trials
Epilepsy, familial adult myoclonic, 1 0 trials
Epilepsy, familial adult myoclonic, 2 0 trials
Epilepsy, familial adult myoclonic, 3 0 trials
Epilepsy, familial adult myoclonic, 4 0 trials
Epilepsy, familial adult myoclonic, 5 0 trials
Epilepsy, familial adult myoclonic, 6 0 trials
Epilepsy, familial adult myoclonic, 7 0 trials

Including sub-types (7) Tagged with Epilepsy, familial adult myoclonic (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