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Inhalational Induction: A Safe Anaesthetic Management in a Patient with Crouzon Syndrome

Crouzon syndrome is a rare genetic disorder involving craniofacial skeleton development. It’s characterized by a triad of cranial deformities: premature craniosynostosis, facial anomalies (mid-facial hypoplasia), and exophthalmia. The anaesthetic management challenges include the presence of a diffi...

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Detalles Bibliográficos
Autores principales: Mohapatra, Sudeep, Dash, Sulochana, Prasant, NVSN, Samal, Soumya, Pattnaik, Shaswat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949027/
https://www.ncbi.nlm.nih.gov/pubmed/36844117
http://dx.doi.org/10.2478/rjaic-2021-0010
Descripción
Sumario:Crouzon syndrome is a rare genetic disorder involving craniofacial skeleton development. It’s characterized by a triad of cranial deformities: premature craniosynostosis, facial anomalies (mid-facial hypoplasia), and exophthalmia. The anaesthetic management challenges include the presence of a difficult airway, history of obstructive sleep apnea, congenital cardiac disorders, hypothermia, blood loss, and venous air embolism. We present the case of an infant with Crouzon syndrome who was scheduled for a ventriculoperitoneal shunt placement managed with inhalational induction.