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Crouzon syndrome - Wikipedia Crouzon syndrome is an autosomal dominant genetic disorder caused by a mutation in a gene on chromosome 10 that controls the body's production of fibroblast growth factor receptor 2 (FGFR2)
Crouzon syndrome | About the Disease | GARD 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 | FACES Online network designed to offer support to individuals and families affected by Crouzon This group offers online discussions and periodic meetings and social events
Crouzon Syndrome - Childrens Hospital of Philadelphia 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 responsible for the abnormal skull fusions
Crouzon Syndrome - Symptoms, Causes, Treatment | NORD Crouzon syndrome, also known as craniofacial dysostosis, is primarily characterized by premature closure of the fibrous joints (cranial sutures) between certain bones in the skull (craniosynostosis) and distinctive facial features
Crouzon Syndrome - Boston Childrens Hospital What is Crouzon syndrome? Crouzon syndrome, also known as craniofacial dysostosis, is a complex genetic birth disorder that may affect a child’s face, skull, and teeth