ORPHA:620139
Non-syndromic unifrontosphenoidal craniosynostosis
Also called Isolated unifrontosphenoidal craniosynostosis, Isolated unilateral sphenofrontal suture synostosis, Non-syndromic unilateral frontosphenoidal 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:620139 is classified under "Bone diseases" in the Orphanet nomenclature.