Apert syndrome: a rare congenital anomaly and experience from a low-resource country: a case report and review of the literature
Abstract Background Apert syndrome is a congenital condition characterized by coronal craniosynostosis, ex-orbitism, midface hypoplasia as well as symmetric syndactyly of both feet and hands. Apert syndrome is linked by autosomal dominant inheritance to fibroblast growth factors receptor gene altera...
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| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Springer
2025-02-01
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| Series: | Journal of Rare Diseases |
| Subjects: | |
| Online Access: | https://doi.org/10.1007/s44162-024-00064-9 |
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