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Craniofacial Dysostosis

Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia.

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Subheadings:

Tree Number(s): C05.116.099.370.231, C05.660.207.231, C16.131.621.207.231

MeSH Unique ID: D003394

Entry Terms:

  • Craniofacial Dysostosis Syndrome
  • Craniofacial Dysostosis Syndromes
  • Craniofacial Dysarthrosis
  • Craniofacial Dysarthroses
  • Dysarthroses, Craniofacial
  • Dysarthrosis, Craniofacial
  • Dysostosis, Craniofacial
  • Craniofacial Dysostoses
  • Dysostoses, Craniofacial
  • Crouzon Disease
  • Craniofacial Dysostosis, Type I
  • Crouzon Craniofacial Dysostosis
  • Craniofacial Dysostosis, Crouzon
  • Craniofacial Dysostosis Type 1
  • Crouzon's Disease
  • Crouzons Disease
  • Crouzon Syndrome

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