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Crouzon Syndrome — Gene Therapy & Clinical Trials | FollowGene

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Home/Diseases/Crouzon Syndrome

Crouzon Syndrome

Prevalence: 1/25000

skeletal

Official·OMIM:123500 Official·ORPHA207

Craniosynostosis and facial anomalies due to FGFR2 gene mutations.

Associated Genes

No gene records found associated with this disease.

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