A Review of Craniofacial Syndromes

Michelle D.  Lingao

doi:10.47895/amp.v51i3.529

A Review of Craniofacial Syndromes

Michelle D. Lingao

DOI:

https://doi.org/10.47895/amp.v51i3.529

Keywords:

craniosynostosis craniofacial syndromes craniosynostosis genes

Abstract

Craniosynostoses are a complex and heterogeneous group of conditions. The purpose of this review is to describe the entity of craniosynostosis and its associated genes along with the ophthalmic and systemic findings. Several genes such as FGFRs, TWIST1, and MSX2 are involved in both syndromic and nonsyndromic craniosynostosis.

References

How to Cite

A Review of Craniofacial Syndromes . Acta Med Philipp [Internet]. 2017 Sep. 29 [cited 2026 Jul. 28];51(3). Available from: https://actamedicaphilippina.upm.edu.ph/index.php/acta/article/view/529

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A Review of Craniofacial Syndromes

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