Benign adult familial myoclonus epilepsy (Q41210): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Epilepsia mioclônica familiar benigna do adulto (BAFME) é uma síndrome epiléptica hereditária caracterizada por tremores corticais de mão, espasmos mioclônicos e convulsões generalizadas ou focais ocasionais com um curso de doença não progressivo ou muito lentamente progressivo, e sem sinais de demência precoce ou ataxia cerebelar. | |||
| description / en | description / en | ||
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. | |||
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 |
||
| 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. |
