Ocular biometric features of pediatric patients with fibroblast growth factor receptor-related syndromic craniosynostosis

Ametropia is reported as a common ophthalmic manifestation in craniosynostosis. We retrospectively compared childhood refractive error and ocular biometric features of fibroblast growth factor receptor (FGFR)-related syndromic craniosynostosis patients with those of non-syndromic craniosynostosis an...

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Detalles Bibliográficos
Autores principales: Lee, Byung Joo, Lee, Kihwang, Chung, Seung Ah, Lim, Hyun Taek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969619/
https://www.ncbi.nlm.nih.gov/pubmed/33731768
http://dx.doi.org/10.1038/s41598-021-85620-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969619/
https://www.ncbi.nlm.nih.gov/pubmed/33731768
http://dx.doi.org/10.1038/s41598-021-85620-9

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