Autosomal recessive Robinow syndrome (Q101943): Difference between revisions

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15 August 2026
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Latest revision as of 18:47, 16 August 2026

Autosomal recessive Robinow syndrome (RRS) is the less common and the more severe type of Robinow syndrome (RS) characterised by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia.
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    English
    Autosomal recessive Robinow syndrome
    Autosomal recessive Robinow syndrome (RRS) is the less common and the more severe type of Robinow syndrome (RS) characterised by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia.

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      CID11:ID_793292660
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      dki-india-ID_793292660
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      Concluído
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      15 August 2026
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