Progressive myoclonic epilepsy type 1 (Q52152): Difference between revisions
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A doença de Unverricht-Lundborg (ULD) é o tipo mais puro e menos grave de epilepsia mioclônica progressiva (PME) e não está associada a déficit cognitivo progressivo. Ela evolui para uma estabilização dos sintomas na idade adulta, com um grau variável de incapacidade permanente, frequentemente grave, que é principalmente devida a mioclonia. | |||
| description / en | description / en | ||
Unverricht-Lundborg disease (ULD) is the purest and least severe type of progressive myoclonus epilepsy (PME), and is not associated with progressive cognitive deficit. It evolves towards a stabilization of symptoms in adulthood, with a varying degree of permanent, often severe, handicap that is mostly due to myoclonus. | |||
Revision as of 23:24, 13 August 2026
Unverricht-Lundborg disease (ULD) is the purest and least severe type of progressive myoclonus epilepsy (PME), and is not associated with progressive cognitive deficit. It evolves towards a stabilization of symptoms in adulthood, with a varying degree of permanent, often severe, handicap that is mostly due to myoclonus.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_150954581 |
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| English | Progressive myoclonic epilepsy type 1 |
Unverricht-Lundborg disease (ULD) is the purest and least severe type of progressive myoclonus epilepsy (PME), and is not associated with progressive cognitive deficit. It evolves towards a stabilization of symptoms in adulthood, with a varying degree of permanent, often severe, handicap that is mostly due to myoclonus. |
