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Jackson-Weiss syndrome

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Description

Jackson-Weiss syndrome (JWS) is an autosomal dominant condition consisting of craniosynostosis characterized by premature fusion of the cranial sutures as well as radiographic anomalies of the feet (summary by Heike et al., 2001).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

17

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Genes

External Links

  • OMIM

    123150

  • Orphanet

    1540

  • HPO
  • Medgen

    C0795998

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