Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Specifically, this syndrome affects the first branchial (or pharyngeal) arch, which is the precursor of the maxilla and mandible.

2021年12月10日 · Crouzon syndrome is a genetic condition where bones in your baby’s skull fuse too soon. Crouzon syndrome is caused by a genetic mutation in the FGFR2 gene.

Crouzon syndrome, also known as craniofacial dysotosis, is a genetic syndrome in which the seams of the skull fuse in abnormally. This affects the shape of the head and face. It is the most common type of syndromic craniosynostosis. Gene mutations are …

2023年8月7日 · Crouzon syndrome is a genetically inherited syndrome characterized by craniosynostosis (premature fusion of coronal sutures) resulting in the skull and facial deformities.

2017年6月22日 · Crouzon syndrome is a rare inherited disorder in which many of the flexible seams (sutures) in a baby’s skull turn to bone and fuse too early. Early fusion of the skull is the hallmark of a ...

Crouzon syndrome is a disorder characterized by early fusion of certain skull bones (craniosynostosis). This prevents normal growth of the skull, which can affect the shape of the head and face.

Crouzon syndrome, also known as craniofacial dysostosis, is a complex genetic birth disorder that may affect a child’s face, skull, and teeth.