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J Pediatr ; 141(6): 833-6, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12461502

ABSTRACT

A protocol was developed for the detection of fatty acid oxidation disorders (FOD) in cases of sudden unexpected death in infancy (SUDI). Tandem mass spectrometry blood acylcarnitine analysis of Guthrie card blood spots was performed. In the first 5 years, 1.2% of Oregon's 247 SUDI cases were identified with FOD, 2 with medium-chain acyl-CoA dehydrogenase deficiency, and one with very long-chain acyl-CoA dehydrogenase deficiency.


Subject(s)
Acyl-CoA Dehydrogenase, Long-Chain/deficiency , Fatty Acids/metabolism , Sudden Infant Death/etiology , Female , Humans , Infant , Infant, Newborn , Male , Mass Spectrometry , Sudden Infant Death/pathology
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