3-hydroxyacyl-CoA dehydrogenase

Results: 57



#Item
11Fatty 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

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

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Source URL: www.albertahealthservices.ca

Language: English - Date: 2013-09-16 18:33:43
12Rare 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

Microsoft Word - SCHADD_update_2013

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Source URL: www.newbornscreening.info

Language: English - Date: 2013-12-01 02:48:45
13Rare 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

Microsoft Word - LCHADD_update_2013

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Source URL: www.newbornscreening.info

Language: English - Date: 2013-12-01 03:02:07
14Fatty-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

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

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Source URL: www.ndhealth.gov

Language: English - Date: 2009-02-19 11:31:59
15Very 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

` NEWBORN SCREENING FACT SHEET VLCADD (Very Long Chain Acyl-CoA Dehydrogenese Deficiency) It is common for babies and children with the

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Source URL: www.ndhealth.gov

Language: English - Date: 2009-02-19 11:32:01
16Medical 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

Microsoft Word - New Hampshire Insert English FINAL.doc

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Source URL: nergg.org

Language: English - Date: 2007-10-17 09:01:06
17Fatty 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

MICHIGAN DEPARTMENT OF COMMUNITY HEALTH BUREAU OF LABORATORIES Newborn Screening – Fatty Acid Oxidation Disorders Rev. Date[removed]

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Source URL: www.michigan.gov

Language: English - Date: 2013-03-15 16:30:13
18Medical 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

Microsoft Word - Rhode Island insert Khmer.doc

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Source URL: nergg.org

Language: English - Date: 2007-10-17 09:01:33
19Fatty 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

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

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Source URL: www.idph.state.ia.us

Language: English - Date: 2007-06-25 16:36:38
20Genetic 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

Delaware Division of Public Health Newborn Screening Program Disorder Name & Abbreviation Analyte / Marker Endocrine Disorder

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Source URL: www.dhss.delaware.gov

Language: English - Date: 2012-07-26 14:33:28
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