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Date: 2013-07-08 12:47:26Genetic genealogy Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Propionic acidemia Malonyl-CoA decarboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine | Newborn Screening Program DisordersAdd to Reading ListSource URL: health.utah.govDownload Document from Source WebsiteFile Size: 56,50 KBShare Document on Facebook |
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What is Carnitine ? Nelson LS Tang, MBChB, FRCPA Associate Professor Department of Chemical Pathology The Chinese University of Hong KongDocID: 13Fs6 - View Document | |
Chart of Metabolic Disorders Screened Table of Disorders Screened by Program Condition IncidenceDocID: Z5KR - View Document | |
physician fact sheet Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency (MCAD) Dr Janice Fletcher, MD, FRACP, BSc, Clinical Geneticist (HGSA), FRCPADocID: W6MK - View Document | |
fact sheet for parents Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency (MCAD) D r J a n i c e F l e t c h e r , MD, FRACP, BSC, Clinical Geneticist (HGSA), FRCPADocID: VUka - View Document |