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An Unoperated Crouzon Family Treated with Monobloc Distraction: Challenges and Lessons

Crouzon syndrome (CS) is a rare form of craniosynostosis characterized by bicoronal craniosynostosis and facial features including severe midface hypoplasia, exophthalmos, and hypertelorism. Most patients are diagnosed and treated in early childhood; however, there are a few reports of Crouzon patie...

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Detalles Bibliográficos
Autores principales: Hart, Justin, Lu, Stephen, Gasteratos, Konstantinos, Chaiyasate, Kongkrit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563069/
https://www.ncbi.nlm.nih.gov/pubmed/34745790
http://dx.doi.org/10.1097/GOX.0000000000003869