ORPHA:3366
Non-syndromic metopic craniosynostosis
Also called Isolated metopic craniosynostosis, Isolated trigonocephaly, Non-syndromic metopic suture synostosis
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal dominant, Not applicable
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- 1-9 / 100 000 (Europe)
- Rarity class
- 1-9 / 100 000
ORPHA:3366 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Trigonocephaly
- Metopic synostosis
- Prominent supraorbital ridges
- Narrow forehead
- Wide nasal bridge
- Hypotelorism