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.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

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)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.