Rapid-onset dystonia-parkinsonism (Q98787): Difference between revisions

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Distonia-parkinsonismo de início rápido (DPR) é um transtorno do movimento caracterizado pelo início abrupto de distonia e parkinsonismo em adultos jovens. É devido a uma mutação no gene ATP1A3. É alélica com hemiplegia alternante da infância.
description / endescription / en
 
Rapid-onset dystonia-parkinsonism (RDP) is a movement disorder characterised by abrupt onset of dystonia and parkinsonism in young adults. It is due to a mutation in the ATP1A3 gene. It is allelic with alternating hemiplegia of childhood.
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Property / Canonical URI: https://id.who.int/icd/entity/878904788 / rank
 
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CID11:ID_878904788
Property / CURIE: CID11:ID_878904788 / rank
 
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dki-india-ID_878904788
Property / Canary Token: dki-india-ID_878904788 / rank
 
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Concluído
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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15 August 2026
Timestamp+2026-08-15T00:00:00Z
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CalendarGregorian
Precision1 day
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Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 15:23, 16 August 2026

Rapid-onset dystonia-parkinsonism (RDP) is a movement disorder characterised by abrupt onset of dystonia and parkinsonism in young adults. It is due to a mutation in the ATP1A3 gene. It is allelic with alternating hemiplegia of childhood.
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ID_878904788
    English
    Rapid-onset dystonia-parkinsonism
    Rapid-onset dystonia-parkinsonism (RDP) is a movement disorder characterised by abrupt onset of dystonia and parkinsonism in young adults. It is due to a mutation in the ATP1A3 gene. It is allelic with alternating hemiplegia of childhood.

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      CID11:ID_878904788
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      dki-india-ID_878904788
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      Concluído
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      15 August 2026
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