Craniofacial Dysostosis

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

Also Known As:

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

Musculoskeletal Diseases: 719
- Bone Diseases: 5863
  - Developmental Bone Diseases: 153
    - Dysostoses: 91
      - Craniofacial Dysostosis: 243
- Musculoskeletal Abnormalities: 43
  - Craniofacial Abnormalities: 203
    - Craniofacial Dysostosis: 243
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Musculoskeletal Abnormalities: 43
    - Craniofacial Abnormalities: 203
      - Craniofacial Dysostosis: 243

Kaplan Plauchu Fitch syndrome

Disease Context: Research Results