Crouzon Syndrome-A Case Report
Crouzon syndrome is a hereditary condition with an autosomal dominant pattern, characterized by the premature synostosis of coronal and sagittal sutures. It ranks as the second most prevalent craniosynostosis syndrome and the results from mutation in FGFR-2 and FGFR-3. We present a case of a 5-year-...
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| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2025-04-01
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| Series: | Journal of Indian Academy of Oral Medicine and Radiology |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/jiaomr.jiaomr_384_24 |
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