Marshall syndrome (Q83115)

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Marshall syndrome is a multisystem autosomal dominant disease characterised by ocular abnormalities, sensorineural hearing loss, craniofacial anomalies and anhidrotic ectodermal dysplasia.
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ID_1401051186
    English
    Marshall syndrome
    Marshall syndrome is a multisystem autosomal dominant disease characterised by ocular abnormalities, sensorineural hearing loss, craniofacial anomalies and anhidrotic ectodermal dysplasia.

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      CID11:ID_1401051186
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      dki-india-ID_1401051186
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      Concluído
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      13 August 2026
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