Crouzon syndrome
ORPHA:207· ICD-10 Q75.1
Definition
Crouzon disease is characterized by craniosynostosis and facial hypoplasia.
- Prevalence
- 1-9 / 1 000 000
- Inheritance
- Autosomal dominant
- Age of onset
- Antenatal, Infancy, Neonatal
ORPHA:207· ICD-10 Q75.1
Crouzon disease is characterized by craniosynostosis and facial hypoplasia.