Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Q88314): Difference between revisions

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Displasia congênita espondiloepimetafisária (SEMD), tipo Strudwick é uma forma de SEMD caracterizada por baixa estatura desproporcional desde o nascimento (com um tronco muito curto e membros encurtados) e anormalidades esqueléticas (lordose, escoliose, vértebras achatadas, tórax carinado, coxa vara, pé torto, e epífises ou metáfises anormais).
description / endescription / en
 
Spondyloepimetaphyseal dysplasia congenita (SEMD), Strudwick type is a form of SEMD characterised by disproportionate short stature from birth (with a very short trunk and shortened limbs) and skeletal abnormalities (lordosis, scoliosis, flattened vertebrae, pectus carinatum, coxa vara, clubfoot, and abnormal epiphyses or metaphyses).
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Property / Canonical URI: https://id.who.int/icd/entity/1090803595 / rank
 
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CID11:ID_1090803595
Property / CURIE: CID11:ID_1090803595 / rank
 
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dki-india-ID_1090803595
Property / Canary Token: dki-india-ID_1090803595 / 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 14:30, 15 August 2026

Spondyloepimetaphyseal dysplasia congenita (SEMD), Strudwick type is a form of SEMD characterised by disproportionate short stature from birth (with a very short trunk and shortened limbs) and skeletal abnormalities (lordosis, scoliosis, flattened vertebrae, pectus carinatum, coxa vara, clubfoot, and abnormal epiphyses or metaphyses).
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ID_1090803595
    English
    Spondyloepimetaphyseal dysplasia congenita, Strudwick type
    Spondyloepimetaphyseal dysplasia congenita (SEMD), Strudwick type is a form of SEMD characterised by disproportionate short stature from birth (with a very short trunk and shortened limbs) and skeletal abnormalities (lordosis, scoliosis, flattened vertebrae, pectus carinatum, coxa vara, clubfoot, and abnormal epiphyses or metaphyses).

      Statements

      CID11:ID_1090803595
      0 references
      dki-india-ID_1090803595
      0 references
      Concluído
      0 references
      13 August 2026
      0 references