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Very long-chain acyl-coenzyme A dehydrogenase deficiency / Fatty-acid metabolism disorder / Hepatology / Hypoglycemia / Carnitine / Newborn screening / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Carnitine-acylcarnitine translocase deficiency / Glycogen storage disease type I / Health / Medicine / Rare diseases
Date: 2009-02-19 11:32:01
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Fatty-acid metabolism disorder
Hepatology
Hypoglycemia
Carnitine
Newborn screening
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Carnitine-acylcarnitine translocase deficiency
Glycogen storage disease type I
Health
Medicine
Rare diseases

` NEWBORN SCREENING FACT SHEET VLCADD (Very Long Chain Acyl-CoA Dehydrogenese Deficiency) It is common for babies and children with the

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