Syndromic craniosynostosis. Craniofacial Surgery. Philadelphia: W. Saunders Company;
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How is Crouzon syndrome inherited? Is there a way to prevent having a child with Crouzon syndrome? How can I find a genetics professional in my area? We hope this information is helpful. We strongly recommend you discuss this information with your doctor.
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Crouzon syndrome is rare disorder characterized by premature craniosynostoses. It carries an autosomal dominant inheritance due to a mutation in fibroblast growth factor receptor 2 FGFR2 gene on chromosome 10q Please Note: You can also scroll through stacks with your mouse wheel or the keyboard arrow keys. Updating… Please wait.