Essential myoclonus (Q41094)
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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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A06.0 |
||
| English | Essential myoclonus |
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. |
Statements
CID11:8A06.0
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dki-india-8A06.0
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Concluído
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13 August 2026
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