![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 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](https://www.pdfsearch.io/img/e87c682d4d1dbfdbcdd84a566b04c58d.jpg) Date: 2009-02-19 11:32:01Very 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 theAdd to Reading ListSource URL: www.ndhealth.govDownload Document from Source Website File Size: 84,18 KBShare Document on Facebook
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