ORPHA:35099

Non-syndromic bicoronal craniosynostosis

Also called Non-syndromic bilateral coronal suture synostosis, Isolated bicoronal craniosynostosis, Isolated synostotic brachycephaly

Body system

Bone diseases

Inheritance pattern

Autosomal dominant, Not applicable

Typical age of onset

Infancy, Neonatal

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:35099 is classified under "Bone diseases" in the Orphanet nomenclature.