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8A06.0 Essential myoclonus

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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.

synonyms

• Essential myoclonus
• Familial essential myoclonus

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