Ataxia due to multiple system atrophy, cerebellar type (Q56403): Difference between revisions

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Atrofia de múltiplos sistemas (AMS) é um transtorno neurodegenerativo de início tardio, esporádico, clinicamente caracterizado por falência autonômica e também por parkinsonismo pouco responsivo à levodopa ou ataxia cerebelar. O subtipo de AMS com predominância de ataxia devido a disfunção cerebelar é denominado de AMS-C.
description / endescription / en
 
Multiple system atrophy (MSA) is a late-onset, sporadic neurodegenerative disorder clinically characterised by autonomic failure and either poorly levodopa-responsive parkinsonism or cerebellar ataxia. The subtype of MSA with predominance of ataxia due to cerebellar dysfunction is called MSA-C.
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Property / Canonical URI: https://id.who.int/icd/entity/572612416 / rank
 
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CID11:ID_572612416
Property / CURIE: CID11:ID_572612416 / rank
 
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dki-india-ID_572612416
Property / Canary Token: dki-india-ID_572612416 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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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 04:05, 14 August 2026

Multiple system atrophy (MSA) is a late-onset, sporadic neurodegenerative disorder clinically characterised by autonomic failure and either poorly levodopa-responsive parkinsonism or cerebellar ataxia. The subtype of MSA with predominance of ataxia due to cerebellar dysfunction is called MSA-C.
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ID_572612416
    English
    Ataxia due to multiple system atrophy, cerebellar type
    Multiple system atrophy (MSA) is a late-onset, sporadic neurodegenerative disorder clinically characterised by autonomic failure and either poorly levodopa-responsive parkinsonism or cerebellar ataxia. The subtype of MSA with predominance of ataxia due to cerebellar dysfunction is called MSA-C.

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      CID11:ID_572612416
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      dki-india-ID_572612416
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      Concluído
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      13 August 2026
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