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Anesthetic Implications in a Child with Crouzon Syndrome

Crouzon syndrome (CS) is an autosomal dominant genetic disorder characterized by craniofacial dysostosis. Premature fusion of skull base leads to midfacial hypoplasia, shallow orbit, mandibular prognathism, overcrowding of upper teeth, high-arched palate, and upper airway obstruction. It is importan...

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Detalles Bibliográficos
Autores principales:	Kumar, Ajeet, Goel, Nitika, Sinha, Chandni, Singh, Abhishek
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341658/ https://www.ncbi.nlm.nih.gov/pubmed/28298794 http://dx.doi.org/10.4103/0259-1162.200234

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