Autosomal dominant cerebellar ataxia type 3 (Q85241): Difference between revisions

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Grupo de ataxias cerebelares autossômicas dominantes denominadas ataxias espinocerebelares (SCA), que são caracterizadas por disartria, reflexos variáveis, rigidez extrapiramidal, distonia, sinais bulbares, fraqueza motora distal, polineuropatia ou oftalmoplegia. Várias estão associados à codificação de expansões de repetição CAG e exibem antecipação genética ao longo das gerações.
description / endescription / en
 
Group of autosomal dominant cerebellar ataxias referred to as spinocerebellar ataxias (SCAs) that are characterized by dysarthria, variable reflexes, extrapyramidal rigidity, dystonia, bulbar signs, distal motor weakness, polyneuropathy, or ophthalmoplegia. Several are associated with coding CAG repeat expansions and display genetic anticipation across generations.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/390406504 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_390406504
Property / CURIE: CID11:ID_390406504 / rank
 
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Property / Canary Token
 
dki-india-ID_390406504
Property / Canary Token: dki-india-ID_390406504 / rank
 
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Property / Verification Status
 
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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Property / Collection date
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 10:36, 15 August 2026

Group of autosomal dominant cerebellar ataxias referred to as spinocerebellar ataxias (SCAs) that are characterized by dysarthria, variable reflexes, extrapyramidal rigidity, dystonia, bulbar signs, distal motor weakness, polyneuropathy, or ophthalmoplegia. Several are associated with coding CAG repeat expansions and display genetic anticipation across generations.
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ID_390406504
    English
    Autosomal dominant cerebellar ataxia type 3
    Group of autosomal dominant cerebellar ataxias referred to as spinocerebellar ataxias (SCAs) that are characterized by dysarthria, variable reflexes, extrapyramidal rigidity, dystonia, bulbar signs, distal motor weakness, polyneuropathy, or ophthalmoplegia. Several are associated with coding CAG repeat expansions and display genetic anticipation across generations.

      Statements

      CID11:ID_390406504
      0 references
      dki-india-ID_390406504
      0 references
      Concluído
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      13 August 2026
      0 references