Dyggve-Melchior-Clausen disease (Q88337): Difference between revisions

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13 August 2026
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Latest revision as of 14:32, 15 August 2026

Dyggve-Melchior-Clausen disease is a rare skeletal disorder belonging to the group of spondyloepimetaphyseal dysplasias (SEMD), and characterised by progressive dwarfism with short trunk, protruding sternum, microcephaly and mental retardation of varying severity.
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ID_21266164
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    Dyggve-Melchior-Clausen disease
    Dyggve-Melchior-Clausen disease is a rare skeletal disorder belonging to the group of spondyloepimetaphyseal dysplasias (SEMD), and characterised by progressive dwarfism with short trunk, protruding sternum, microcephaly and mental retardation of varying severity.

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      CID11:ID_21266164
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      dki-india-ID_21266164
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      Concluído
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      13 August 2026
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