ORPHA:35093

Non-syndromic sagittal craniosynostosis

Also called Isolated sagittal craniosynostosis, Isolated scaphocephaly, Non-syndromic sagittal suture synostosis

Body system

Bone diseases

Inheritance pattern

Autosomal dominant, Not applicable

Typical age of onset

Infancy, Neonatal

Estimated prevalence

1-5 / 10 000 (Australia)

Rarity class

1-5 / 10 000

ORPHA:35093 is classified under "Bone diseases" in the Orphanet nomenclature.