Digitotalar dysmorphism (Q104859): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/1679749810 / rank
 
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CID11:ID_1679749810
Property / CURIE: CID11:ID_1679749810 / rank
 
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dki-india-ID_1679749810
Property / Canary Token: dki-india-ID_1679749810 / 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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16 August 2026
Timestamp+2026-08-16T00:00:00Z
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CalendarGregorian
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Property / Collection date: 16 August 2026 / rank
 
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Latest revision as of 10:43, 17 August 2026

Digitotalar dysmorphism or distal arthrogryposis type 1 is an autosomal dominant congenital anomaly characterised by contractures of the distal regions of the hands and feet with no additional anomalies. It is the most common type of distal arthrogryposis. Expressivity is variable and patients may present camptodactyly, clasped thumbs without extension, overriding fingers, ulnar deviation of the fingers, clubfoot, vertical talus. Facial involvement is typically absent. The hands are most frequently involved than the feet. Multiple genes encoding proteins in the sarcomere have been implicated.
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ID_1679749810
    English
    Digitotalar dysmorphism
    Digitotalar dysmorphism or distal arthrogryposis type 1 is an autosomal dominant congenital anomaly characterised by contractures of the distal regions of the hands and feet with no additional anomalies. It is the most common type of distal arthrogryposis. Expressivity is variable and patients may present camptodactyly, clasped thumbs without extension, overriding fingers, ulnar deviation of the fingers, clubfoot, vertical talus. Facial involvement is typically absent. The hands are most frequently involved than the feet. Multiple genes encoding proteins in the sarcomere have been implicated.

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      CID11:ID_1679749810
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      dki-india-ID_1679749810
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      Concluído
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      16 August 2026
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