Crouzon syndrome in a fraternal twin: A case report and review of the literature

BACKGROUND: Crouzon syndrome (CS; OMIM 123500) is an autosomal dominant inherited craniofacial disorder caused by mutations in the fibroblast growth factor receptor 2 (FGFR2) gene. CS is characterized by craniofacial dysostosis, exophthalmos, and facial anomalies with hypoplastic maxilla and relativ...

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Detalles Bibliográficos
Autores principales: Li, Xiao-Jing, Su, Ji-Mei, Ye, Xiao-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9210876/
https://www.ncbi.nlm.nih.gov/pubmed/35812652
http://dx.doi.org/10.12998/wjcc.v10.i16.5317

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9210876/
https://www.ncbi.nlm.nih.gov/pubmed/35812652
http://dx.doi.org/10.12998/wjcc.v10.i16.5317

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