Variants
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Sweeney-Cox syndrome

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Description

Sweeney-Cox syndrome is characterized by striking facial dysostosis, including hypertelorism, deficiencies of the eyelids and facial bones, cleft palate/velopharyngeal insufficiency, and low-set cupped ears (Kim et al., 2017).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

3

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Genes

External Links

  • OMIM

    617746

  • Orphanet
  • HPO
  • Medgen

    C4540299

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