Benign adult familial myoclonus epilepsy (Q41210): Difference between revisions
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Revision as of 07:17, 13 August 2026
Benign adult familial myoclonic epilepsy (BAFME) is an inherited epileptic syndrome characterised by cortical hand tremors, myoclonic jerks and occasional generalised or focal seizures with a non-progressive or very slowly progressive disease course, and no signs of early dementia or cerebellar ataxia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A61.32 |
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| English | Benign adult familial myoclonus epilepsy |
Benign adult familial myoclonic epilepsy (BAFME) is an inherited epileptic syndrome characterised by cortical hand tremors, myoclonic jerks and occasional generalised or focal seizures with a non-progressive or very slowly progressive disease course, and no signs of early dementia or cerebellar ataxia. |
Statements
CID11:8A61.32
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