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

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A síndrome de displasia espondilometafisária - distrofia de cone e bastonete é caracterizada pela associação de displasia espondilometafisária (marcada por platispondilia, encurtamento dos ossos tubulares e irregularidade e escavação metafisárias progressivas), com retardo de crescimento pós-natal e comprometimento visual progressivo devido à distrofia de cone e bastonete.
description / endescription / en
 
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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Property / Canonical URI: https://id.who.int/icd/entity/430156722 / rank
 
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CID11:ID_430156722
Property / CURIE: CID11:ID_430156722 / rank
 
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dki-india-ID_430156722
Property / Canary Token: dki-india-ID_430156722 / 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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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 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.

      Statements

      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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