Progressive myoclonic epilepsy type 1 (Q52152): Difference between revisions
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13 August 2026
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Latest 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. |
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CID11:ID_150954581
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dki-india-ID_150954581
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Concluído
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13 August 2026
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