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Article

Ocular manifestations and treatment progress of Crouzon syndrome.

International ophthalmology - 5 Sept 2024

Huang Shuting, Zhang Dengfeng, Li Bei

Abstract excerpt

PURPOSE: Crouzon syndrome is a congenital genetic disease caused by mutations of the FGFR2 gene on chromosome 10. It is usually inherited in an autosomal dominant pattern and is one of the most common types of craniosynostosis syndromes. This article focuses on the ophthalmology-related aspects of Crouzon syndrome in order to help diagnose and develop personalized treatment plans. METHODS: A combined systematic...

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PMID: 39235629
DOI: 10.1007/s10792-024-03293-5

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