ORPHA:207
Crouzon syndrome
Also called Crouzon craniofacial dysostosis
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Antenatal, Infancy, Neonatal
- Estimated prevalence
- 1-9 / 1 000 000 (Europe)
- Rarity class
- 1-9 / 1 000 000
ORPHA:207 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- High forehead
- Abnormal skull morphology
- Abnormal facial shape
- Frontal bossing
- Multiple suture craniosynostosis
- Brachycephaly