Essential myoclonus (Q41094): Difference between revisions
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Forma hereditária de mioclonia, que não está usualmente associada a epilepsia ou a qualquer outra condição clínica. Mioclonia essencial tende a ser estável sem piorar de gravidade ao longo do tempo. Mais recentemente, acredita-se que a mioclonia essencial pode ser o mesmo que a distonia-mioclônica causada por uma mutação no gene sarcoglicano. | |||
| description / en | description / en | ||
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. | |||
Revision as of 07:09, 13 August 2026
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 |
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| 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. |
