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Date: 2014-03-27 09:48:48Newborn screening Congenital adrenal hyperplasia Galactosemia Phenylketonuria Biotinidase deficiency Congenital hypothyroidism 3-Methylcrotonyl-CoA carboxylase deficiency Inborn error of metabolism 2-Methylbutyryl-CoA dehydrogenase deficiency Health Medicine Pediatrics | Title 15 - Mississippi Department of HealthAdd to Reading ListSource URL: www.msdh.state.ms.usDownload Document from Source WebsiteFile Size: 102,47 KBShare Document on Facebook |
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NEWBORN SCREENING FACT SHEET 2MBDH Deficiency (2-Methylbutyryl CoA Dehydrogenase Deficiency) What is it? 2MBDH deficiency is one type of organic acid disorder. People with 2MBDH deficiency haveDocID: zAyL - View Document |