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Beare-Stevenson Cutis Gyrata Syndrome
A syndrome that is characterized by cutis gyrata, acanthosis nigricans and craniosynostosis, is caused by heterozygous mutation in the FGFR2 gene on chromosome 10q26.
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
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
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Overview
A syndrome that is characterized by cutis gyrata, acanthosis nigricans and craniosynostosis, is caused by heterozygous mutation in the FGFR2 gene on chromosome 10q26.
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.