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

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13 August 2026
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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
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    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).

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