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 / endescription / 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.
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Property / Canonical URI: https://id.who.int/icd/entity/150954581 / rank
 
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CID11:ID_150954581
Property / CURIE: CID11:ID_150954581 / rank
 
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Property / Canary Token
 
dki-india-ID_150954581
Property / Canary Token: dki-india-ID_150954581 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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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.
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ID_150954581
    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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