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3-hydroxyacyl-CoA dehydrogenase
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11	Long Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency (metabolic condition: fatty acid oxidation disorder) Also known as: • long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency • long-chain 3-OH acy Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:33:43 Fatty acids Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Mitochondrial trifunctional protein deficiency 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hydroxyacyl-Coenzyme A dehydrogenase Fatty acid metabolism Mitochondrial trifunctional protein ACADL Health Chemistry Medicine
12	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
13	Microsoft Word - LCHADD_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-12-01 03:02:07 Rare diseases Fatty acids Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Mitochondrial trifunctional protein deficiency 3-hydroxyacyl-coenzyme A dehydrogenase deficiency 3-hydroxyacyl-CoA dehydrogenase Newborn screening Fatty acid metabolism Health Medicine Biology
14	NEWBORN SCREENING FACT SHEET LCHADD (Long Chain 3-Hydroxyacyl-CoA Dehydrogenese Deficiency) What is it? LCHADD stands for long chain 3-hydroxyacylCoA dehydrogenase deficiency. It is one type of fatty acid oxidation disor Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:59 Fatty-acid metabolism disorder Hepatology Hypoglycemia Mitochondrial trifunctional protein deficiency Carnitine Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Newborn screening Adipose tissue Carnitine-acylcarnitine translocase deficiency Health Medicine Rare diseases
15	` NEWBORN SCREENING FACT SHEET VLCADD (Very Long Chain Acyl-CoA Dehydrogenese Deficiency) It is common for babies and children with the Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:32:01 Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Hepatology Hypoglycemia Carnitine Newborn screening Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Glycogen storage disease type I Health Medicine Rare diseases
16	Microsoft Word - New Hampshire Insert English FINAL.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:01:06 Medical genetics Newborn screening 3-Methylcrotonyl-CoA carboxylase deficiency Methylcrotonyl-CoA carboxylase Propionic acidemia Biotinidase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Thiolase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
17	MICHIGAN DEPARTMENT OF COMMUNITY HEALTH BUREAU OF LABORATORIES Newborn Screening – Fatty Acid Oxidation Disorders Rev. Date[removed] Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2013-03-15 16:30:13 Fatty acids Fatty-acid metabolism disorder Newborn screening Thiolase 2 4 Dienoyl-CoA reductase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Carnitine Health Medicine Chemistry
18	Microsoft Word - Rhode Island insert Khmer.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:01:33 Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Mitochondrial trifunctional protein deficiency Methylcrotonyl-CoA 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Genetic genealogy
19	Disease Name LONG-CHAIN HYDROXYACYL-CoA DEHYDROGENASE (LCHAD) (LCHAD; MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFECT; LONG-CHAIN HYDROXYACYL-CoA DEHYDROGENASE; LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY) Fatty aci Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:38 Fatty acids Metabolism Mitochondrial trifunctional protein Proteins Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Hepatology Hydroxyacyl-Coenzyme A dehydrogenase HADHA Biology Health Chemistry
20	Delaware Division of Public Health Newborn Screening Program Disorder Name & Abbreviation Analyte / Marker Endocrine Disorder Add to Reading List Source URL: www.dhss.delaware.gov Language: English - Date: 2012-07-26 14:33:28 Genetic genealogy Newborn screening Carnitine Fatty-acid metabolism disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Methylmalonic acidemia Glutaric acidemia type 2 Acyl CoA dehydrogenase Health Rare diseases Medicine

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