Rare Zebra

Rare disease search prototype built on Orphanet data

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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