Anesthetic management of craniosynostosis repair in patient with Apert syndrome

Apert syndrome is an autosomal dominant disease characterized by craniosynostosis, midface hypoplasia and syndactyly. In general, patients present in early childhood for craniofacial reconstruction surgery. Anesthetic implications include difficult airway, airway hyper-reactivity; however, possibili...

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Detalles Bibliográficos
Autores principales: Kumar, Niraj, Arora, Shubhangi, Bindra, Ashish, Goyal, Keshav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141395/
https://www.ncbi.nlm.nih.gov/pubmed/25191197
http://dx.doi.org/10.4103/1658-354X.136631

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141395/
https://www.ncbi.nlm.nih.gov/pubmed/25191197
http://dx.doi.org/10.4103/1658-354X.136631

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