Abstract
DiGeorge syndrome is associated with a chromosome 22q11.2 deletion and manifests with variable clinical findings. Aspiration pneumonia can be a perioperative complication of great concern in this syndrome. In this report, we present a case of a 16-month old child with DiGeorge syndrome undergoing cranioplasty. He developed perioperative aspiration pneumonia but was managed successfully. © the Korean Society of Anesthesiologists, 2011.
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Lee, J. Y., & Han, Y. J. (2011). Aspiration pneumonia in the child with DiGeorge syndrome -A case report-. Korean Journal of Anesthesiology, 60(6), 449–452. https://doi.org/10.4097/kjae.2011.60.6.449
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