ORPHA:620192
Non-syndromic metopic and sagittal craniosynostosis
Also called Isolated metopic and sagittal craniosynostosis, Non-syndromic metopic and sagittal suture synostosis
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:620192 is classified under "Bone diseases" in the Orphanet nomenclature.