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Crouzon Syndrome-Acanthosis Nigricans Syndrome
A syndrome characterized by Crouzon-like features, premature synostosis of cranial sutures, and acanthosis nigricans that is caused by heterozygous missense mutation in the FGFR3 gene on chromosome 4p16.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
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Overview
A syndrome characterized by Crouzon-like features, premature synostosis of cranial sutures, and acanthosis nigricans that is caused by heterozygous missense mutation in the FGFR3 gene on chromosome 4p16.
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