ORPHA:620102
Non-syndromic unicoronal craniosynostosis
Also called Isolated frontal plagiocephaly, Isolated unicoronal craniosynostosis, Non-syndromic anterior synostotic plagiocephaly, Non-syndromic frontoparietal craniosynostosis, Non-syndromic hemicoronal craniosynostosis, Non-syndromic unilateral coronal synostosis
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Neonatal
- Estimated prevalence
- 1-9 / 1 000 000 (Worldwide)
- Rarity class
- 1-9 / 1 000 000
ORPHA:620102 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Abnormality of the forehead
- Torticollis
- Astigmatism
- Strabismus
- Amblyopia
- Frontal bossing