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Management of general anesthesia in an infant with duplication 3Q syndrome and medium-chain ACYL-COA dehydrogenase deficiency

✍ Scribed by Christopher Chu; William Flexer


Publisher
Springer-Verlag
Year
2008
Tongue
French
Weight
14 KB
Volume
55
Category
Article
ISSN
1496-8975

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## Abstract We report on a 6‐year‐old girl who presented at 6 months of age with seizures, delayed psychomotor development and mild facial dysmorphism. A small muscular ventricular septal defect was documented on echocardiogram and brain MRI showed a frontal brain anomaly. Urine organic acid analys