Spondylometaphyseal dysplasia - cone-rod dystrophy (Q63005): Difference between revisions

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13 August 2026
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Latest revision as of 10:29, 14 August 2026

Spondylometaphyseal dysplasia - cone-rod dystrophy syndrome is characterised by the association of spondylometaphyseal dysplasia (marked by platyspondyly, shortening of the tubular bones and progressive metaphyseal irregularity and cupping), with postnatal growth retardation and progressive visual impairment due to cone-rod dystrophy.
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ID_430156722
    English
    Spondylometaphyseal dysplasia - cone-rod dystrophy
    Spondylometaphyseal dysplasia - cone-rod dystrophy syndrome is characterised by the association of spondylometaphyseal dysplasia (marked by platyspondyly, shortening of the tubular bones and progressive metaphyseal irregularity and cupping), with postnatal growth retardation and progressive visual impairment due to cone-rod dystrophy.

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      CID11:ID_430156722
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      dki-india-ID_430156722
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      Concluído
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      13 August 2026
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