Catalog

Essential myoclonus

8A06.0

Link to WHO Definition

Essential myoclonus – http://id.who.int/icd/entity/179893645

This is a hereditary form of myoclonus, which is not usually associated with epilepsy or any other medical condition. Essential myoclonus tends to be stable without increasing in severity over time. More recently, it is believed that essential myoclonus may be the same as myoclonus-dystonia caused by a mutation in the sarcoglycan gene.

Parents