Chondrodystrophic myotonia (Q41391): Difference between revisions

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Miotonia condrodistrófica (síndrome de Schwartz-Jampel) é uma síndrome miotônica congênita caracterizada por miotonia que resulta em uma fácies característica com blefarofimose e uma aparência facial enrugada, e anormalidades osteoarticulares que levam à mobilidade articular limitada.
description / endescription / en
 
Chondrodystrophic myotonia (Schwartz-Jampel syndrome) is a congenital myotonic syndrome characterised by myotonia that results in a characteristic facies with blepharophimosis and a puckered facial appearance, and osteoarticular abnormalities leading to limited joint mobility.
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Property / Canonical URI: https://id.who.int/icd/entity/1725668060 / rank
 
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Property / CURIE
 
CID11:8C71.1
Property / CURIE: CID11:8C71.1 / rank
 
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Property / Canary Token
 
dki-india-8C71.1
Property / Canary Token: dki-india-8C71.1 / 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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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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Property / Linked ICD 10
 
Property / Linked ICD 10: G71.1 / rank
 
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Latest revision as of 07:32, 13 August 2026

Chondrodystrophic myotonia (Schwartz-Jampel syndrome) is a congenital myotonic syndrome characterised by myotonia that results in a characteristic facies with blepharophimosis and a puckered facial appearance, and osteoarticular abnormalities leading to limited joint mobility.
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8C71.1
    English
    Chondrodystrophic myotonia
    Chondrodystrophic myotonia (Schwartz-Jampel syndrome) is a congenital myotonic syndrome characterised by myotonia that results in a characteristic facies with blepharophimosis and a puckered facial appearance, and osteoarticular abnormalities leading to limited joint mobility.

      Statements

      CID11:8C71.1
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      dki-india-8C71.1
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      Concluído
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      13 August 2026
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