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Middle East J Anaesthesiol ; 21(3): 419-21, 2011 Oct.
Article in English | MEDLINE | ID: mdl-22428500

ABSTRACT

Cornelia De Lange syndrome is a rare genetically heterogeneous and sporadic syndrome, with an estimated prevalence of 1 in 10,000 to 30,000. The disorder may present many complications during anesthesia due to cardiac, gastrointestinal and airway anomalies. We report a case of an ex premature toddler presenting for repair of a cleft palate. Postoperatively she had respiratory distress, successfully treated by the anesthetic care team Causes for the complication are discussed.


Subject(s)
Cleft Palate/surgery , De Lange Syndrome/surgery , Postoperative Complications/etiology , Respiratory Tract Diseases/etiology , Anesthesia/adverse effects , Anesthesia, Inhalation , Female , Gastrointestinal Tract/abnormalities , Heart Defects, Congenital/complications , Humans , Infant , Infant, Newborn , Infant, Premature , Postoperative Complications/therapy , Respiratory Distress Syndrome/etiology , Respiratory Distress Syndrome/therapy , Respiratory System Abnormalities/complications , Respiratory Tract Diseases/therapy
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