Craniofacial Dysostosis

It is feasible that the primary title of the record Crouzon Disorder is not the name you expected. Kindly examine the basic synonyms listing to find the alternating name(s) and also disorder subdivision(s) covered by this report.


  • Craniofacial Dysostosis
  • Crouzon Craniofacial Dysostosis
  • Craniostenosis, Crouzon Type

Condition Communities

  • Oxycephaly-Acrocephaly
  • Virchow’s Oxycephaly

General Conversation
Crouzon syndrome is a rare genetic disorder that may appear at birth (hereditary) or during early stage. The condition is identified by unique malformations of the skull and facial (craniofacial) area. Such abnormalities may vary considerably in range as well as seriousness from case to instance, including among influenced member of the family. Nonetheless, in a lot of babies with Crouzon syndrome, the coarse joints between certain bones of the head (cranial stitches) close too soon (craniosynostosis). In addition, facial irregularities normally include unusual protruding or protrusion of the eyeballs (proptosis) as a result of shallow eye tooth cavities (orbits); external deviation of one of the eyes (different strabismus or exotropia); commonly spaced eyes (ocular hypertelorism); and also a small, underdeveloped top mouth (hypoplastic maxilla), with protrusion of the lower jaw (loved one mandibular prognathism).

In some circumstances, Crouzon disorder is inherited as an autosomal leading characteristic. In other situations, impacted people have no family members history of the disease. In such instances, Crouzon syndrome is thought to arise from new hereditary modifications (mutations) that take place randomly for unidentified factors (occasionally).

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