![2-Methylbutyryl-CoA dehydrogenase deficiency / 2-Methylbutyryl-CoA / Newborn screening / Hypoglycemia / Carnitine / Health / Medicine / Rare diseases 2-Methylbutyryl-CoA dehydrogenase deficiency / 2-Methylbutyryl-CoA / Newborn screening / Hypoglycemia / Carnitine / Health / Medicine / Rare diseases](https://www.pdfsearch.io/img/1ce11defc15e11ada7b44372ec6de041.jpg) Date: 2007-06-25 16:35:432-Methylbutyryl-CoA dehydrogenase deficiency 2-Methylbutyryl-CoA Newborn screening Hypoglycemia Carnitine Health Medicine Rare diseases | | Disease Name 2-METHYLBUTYRYL-CoA DEHYDROGENASE DEFICIENCY (2MBCD) (SHORT/BRANCHED CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY; 2METHYLBUTYRYLGLYCINURIA) Organic aciduria and fatty acid oxidation defect. Classification: InherAdd to Reading ListSource URL: www.idph.state.ia.usDownload Document from Source Website File Size: 21,43 KBShare Document on Facebook
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