Primary Dystonia DYT1 Type (Q86086): Difference between revisions

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Distonia primária do tipo DYT1 é causada por uma mutação no gene da torsina. É mais comum em pessoas de descendência judaica Askanazi. O início ocorre na infância com envolvimento da perna que se espalha para outras partes do corpo.
description / endescription / en
 
Primary dystonia of DYT 1 type is caused by a mutation in the torsion gene. It is more common in people of Askanazi Jewish descent. The onset is in childhood with leg involvement that spreads to other body parts.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/300062534 / rank
 
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Property / CURIE
 
CID11:ID_300062534
Property / CURIE: CID11:ID_300062534 / rank
 
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Property / Canary Token
 
dki-india-ID_300062534
Property / Canary Token: dki-india-ID_300062534 / 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
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After0
Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 11:27, 15 August 2026

Primary dystonia of DYT 1 type is caused by a mutation in the torsion gene. It is more common in people of Askanazi Jewish descent. The onset is in childhood with leg involvement that spreads to other body parts.
Language Label Description Also known as
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ID_300062534
    English
    Primary Dystonia DYT1 Type
    Primary dystonia of DYT 1 type is caused by a mutation in the torsion gene. It is more common in people of Askanazi Jewish descent. The onset is in childhood with leg involvement that spreads to other body parts.

      Statements

      CID11:ID_300062534
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      dki-india-ID_300062534
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      Concluído
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      13 August 2026
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