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Acyl-CoA dehydrogenase
Results: 122

#	Item
81	Parent Fact Sheet Disorder Short Chain Acyl-CoA Dehydrogenase Deficiency (SCAD) Cause People with Short Chain Acyl-CoA Dehydrogenase deficiency have problems breaking down fat into energy for their body. Most babies with Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-09 14:33:51 Rare diseases Coenzymes Metabolism Carnitine Newborn screening Riboflavin Acyl CoA dehydrogenase Acyl-CoA Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Chemistry Biology
82	PARENT FACT SHEET DISORDER Medium-chain acyl-CoA dehydrogenase deficiency (MCAD) CAUSE MCAD occurs when an enzyme called “medium chain acyl-CoA dehydrogenase” is either missing or not working Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 07:58:17 Chemistry Hypoglycemia Metabolism Carnitine Fatty-acid metabolism disorder Very long-chain acyl-coenzyme A dehydrogenase deficiency Medicine Health Medium-chain acyl-coenzyme A dehydrogenase deficiency
83	PARENT FACT SHEET Very long-chain acyl-CoA dehydrogenase deficiency (VLCAD) CAUSE VLCAD occurs when the very long chain acyl-CoA dehydrogenase enzyme is missing or not working properly. This enzyme’s job is to break do Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-09 02:37:56 Very long-chain acyl-coenzyme A dehydrogenase deficiency Rare diseases Newborn screening Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Carnitine Metabolism Acyl CoA dehydrogenase Acyl-CoA ACADVL Health Chemistry Medicine
84	Newborn Screening Brochure Add to Reading List Source URL: www.wadsworth.org Language: English - Date: 2011-10-11 08:14:49 Genetic genealogy Newborn screening Methylmalonic acidemia Propionic acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Isovaleric acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Health Rare diseases Medicine
85	Baby is Home! KIDSNET All babies born in Rhode Island are enrolled in KIDSNET, the Rhode Island information system that helps families and doctors make sure that Add to Reading List Source URL: www.nergg.org Language: English - Date: 2012-04-06 15:58:29 Genetic genealogy Newborn screening Phenylketonuria Methylmalonic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Propionic acidemia Isovaleric acidemia Health Rare diseases Medicine
86	STATE OF NEW HAMPSHIRE DEPARTMENT OF HEALTH AND HUMAN SERVICES Nicholas A. Toumpas Commissioner Add to Reading List Source URL: www.dhhs.state.nh.us Language: English - Date: 2014-08-08 09:16:27 Newborn screening Propionic acidemia Methylmalonic acidemia Acyl CoA dehydrogenase Medium-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency Isovaleric acidemia Carnitine palmitoyltransferase I 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Medicine
87	State of Illinois Rod R. Blagojevich, Governor Department of Public Health Eric E. Whitaker, M.D., M.P.H., Director Newborn Metabolic Add to Reading List Source URL: www.idph.state.il.us Language: English - Date: 2007-07-24 10:41:11 Medical genetics Newborn screening Propionic acidemia Fatty-acid metabolism disorder 2-Methylbutyryl-CoA dehydrogenase deficiency Biotinidase deficiency Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Health Rare diseases Genetic genealogy
88	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2009-02-03 16:51:23 Medical genetics Argininosuccinic aciduria Urea cycle disorder Newborn screening Argininosuccinate lyase Carbamoyl phosphate synthetase I deficiency Glutaric acidemia type 2 Health Rare diseases Genetic genealogy
89	Microsoft Word - 3MCC.doc Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-09 15:58:40 3-Methylcrotonyl-CoA carboxylase deficiency Carnitine Rare diseases Amino acid Protein Very long-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Health Chemistry Medicine
90	MCAD - Carson and Brynn: A Family’s Story We live in Phoenix, AZ and have two kids with Medium-chain acyl-CoA dehydrogenase deficiency (MCAD), Carson (age 9) and Brynn (age 4). Carson was born in 2004 and at that time Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2013-08-16 18:53:50 Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Medicine Health Pediatrics Epidemiology

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