Dementia due to familial Creutzfeldt-Jakob disease (Q57813): Difference between revisions

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Demência devida a uma forma genética da doença de Creutzfeldt-Jakob, envolvendo uma mutação no gene da proteína priônica. É autossômica dominante e pode se apresentar com um curso rápido ou mais lentamente progressivo.
description / endescription / en
 
Dementia due to a genetic form of Creutzfeldt-Jakob disease involving a mutation in the prion protein gene. It is autosomal dominant and can present with a rapid or more slowly progressive course.
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Property / Canonical URI: https://id.who.int/icd/entity/1967143045 / rank
 
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CID11:ID_1967143045
Property / CURIE: CID11:ID_1967143045 / rank
 
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dki-india-ID_1967143045
Property / Canary Token: dki-india-ID_1967143045 / 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 05:26, 14 August 2026

Dementia due to a genetic form of Creutzfeldt-Jakob disease involving a mutation in the prion protein gene. It is autosomal dominant and can present with a rapid or more slowly progressive course.
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ID_1967143045
    English
    Dementia due to familial Creutzfeldt-Jakob disease
    Dementia due to a genetic form of Creutzfeldt-Jakob disease involving a mutation in the prion protein gene. It is autosomal dominant and can present with a rapid or more slowly progressive course.

      Statements

      CID11:ID_1967143045
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      dki-india-ID_1967143045
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      Concluído
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      13 August 2026
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