Crouzon Syndrome Spanning Three Generations: Advances in the Treatment of Syndromic Midface Deficiency

BACKGROUND: Crouzon syndrome is an autosomal dominant genetic disorder characterized by craniosynostosis, midface retrusion, and exophthalmos. Over the past century, the treatment of craniofacial disorders like Crouzon syndrome has evolved significantly. METHODS: An institutional review board–approv...

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Detalles Bibliográficos
Autores principales: Harmon, Kelly A., Ferraro, Jennifer, Rezania, Nikki, Carmona, Taly, Figueroa, Alvaro A., Tragos, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Craniofacial/Pediatric
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684202/
https://www.ncbi.nlm.nih.gov/pubmed/38033876
http://dx.doi.org/10.1097/GOX.0000000000005296

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684202/
https://www.ncbi.nlm.nih.gov/pubmed/38033876
http://dx.doi.org/10.1097/GOX.0000000000005296

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