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Acyl-CoA
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31	EXPANDED NEWBORN SCREENING 2005 to 2009 MISSED OPPORTUNITIES -- POTENTIAL LEGAL CLAIMS Over the past five years, it’s become clear that many children who should have had the benefit of expanded screening did not. By ea Add to Reading List Source URL: fodsupport.org Language: English - Date: 2012-05-31 13:41:05 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Malonyl-CoA decarboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
32	Newborn_Screening_C4.indd Add to Reading List Source URL: www.mayomedicallaboratories.com Language: English - Date: 2014-10-28 14:15:46 Medicine Epidemiology Newborn screening Pediatrics Carnitine Isobutyryl-CoA Acyl CoA dehydrogenase Ethylmalonic encephalopathy Health Chemistry Rare diseases
33	MCAD: Sudden and Unexpected Death of a 45-year-old Woman Kimiyo Raymond, MD, Allen E. Bale, MD, C. Allan Barnes, MD, Piero Rinaldo, MD, PhD Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is the most common fatty a Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:07 Metabolism Fatty acids Fatty-acid metabolism disorder Hepatology Medium-chain acyl-coenzyme A dehydrogenase deficiency Rare diseases Carnitine Fatty acid metabolism Newborn screening Health Medicine Chemistry
34	Example of VLCAD Protocol To Whom It May Concern: Re: (Name of child) Date of Birth: _____________ is a __ year old boy with very long chain acyl-CoA dehydrogenase (VLCAD) deficiency, an inborn error of mitochondrial fat Add to Reading List Source URL: fodsupport.org Language: English - Date: 2012-05-31 13:41:18 Health Nephrology Very long-chain acyl-coenzyme A dehydrogenase deficiency Acute kidney injury Anuria Renal failure Heart failure Myoglobinuria Cardiomyopathy Medicine Anatomy Organ failure
35	Exercise and rhabdomyolysis in long chain fa4y acid oxida5on disorders Cary O. Harding, MD Molecular & Medical Gene5cs Acknowledgements Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-08-13 16:11:50 Metabolism Biochemistry Acyl-CoA Acetyl-CoA Thiolase Very long-chain acyl-coenzyme A dehydrogenase deficiency Acyl CoA dehydrogenase Coenzyme A Beta oxidation Chemistry Biology Coenzymes
36	Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency (metabolic condition: fatty acid oxidation disorder) Also known as: • medium-chain acyl-coenzyme A dehydrogenase deficiency • ACADM deficiency Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:33:57 Fatty acids Fatty-acid metabolism disorder Rare diseases ACADM Medical genetics Hypoglycemia Fatty acid metabolism Carnitine Inborn error of lipid metabolism Medicine Health Medium-chain acyl-coenzyme A dehydrogenase deficiency
37	Newborn_Screening_C8.indd Add to Reading List Source URL: www.mayomedicallaboratories.com Language: English - Date: 2013-09-19 17:08:41 Medium-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Dicarboxylic acid Carnitine Acyl CoA dehydrogenase Acyl-CoA Inborn error of lipid metabolism Chemistry Health Medicine
38	Microsoft Word - SCHADD_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-12-01 02:48:45 Rare diseases Fatty acids Fatty-acid metabolism disorder 3-hydroxyacyl-coenzyme A dehydrogenase deficiency 3-hydroxyacyl-CoA dehydrogenase Newborn screening Hydroxyacyl-Coenzyme A dehydrogenase Fatty acid metabolism Acyl CoA dehydrogenase Chemistry Health Medicine
39	Nutrition and Mitochondrial Fatty Acid Oxidation Defects Phyllis B. Acosta, DrPH, RD INTRODUCTION Three forms of energy (fuel) are used by the body: glucose, fatty acids and ketone bodies. Glucose, after eating and until Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:17 Medicine Fatty acids Hepatology Fatty acid metabolism Carnitine Lipid Glycogen Triglyceride Acyl-CoA Biology Chemistry Metabolism
40	An Educator’s Guide to MCADD What is MCADD? Medium chain acyl-CoA dehydrogenase deficiency (MCADD) Background Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:07 Genetic genealogy Hypoglycemia Inborn errors of carbohydrate metabolism Fatty-acid metabolism disorder Blood sugar Medium-chain acyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Glycogen storage disease type I Medicine Health Diabetes