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3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Results: 111

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71	Microsoft Word - VLCAD.doc Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2007-09-14 09:09:50 Medical genetics Fatty-acid metabolism disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Newborn screening Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
72	Minnesota Department of Health[removed]VLCAD Action required Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:24 Rare diseases Carnitine Very long-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Hypoglycemia Acyl-CoA Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Inborn error of lipid metabolism Health Medicine Chemistry
73	Microsoft Word - FAOD.doc Add to Reading List Source URL: health.tn.gov Language: English - Date: 2007-05-01 14:47:24 Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Mitochondrial trifunctional protein deficiency Newborn screening Lipid Health Medicine Rare diseases
74	Medium chain acyl-CoA Dehydrogenase Deficiency (MCADD) Add to Reading List Source URL: health.tn.gov Language: English - Date: 2007-05-01 10:02:30 Hepatology Metabolism Fatty acids Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
75	Parent Fact Sheet Disorder Long Chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) Cause People with LCHADD have problems breaking down a fatty acid into energy for the body. LCHADD occurs when an enzyme called lo Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 05:28:49 Diabetes Hepatology Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hypoglycemia 3-hydroxyacyl-CoA dehydrogenase 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Blood sugar Very long-chain acyl-coenzyme A dehydrogenase deficiency Glycogen storage disease type I Medicine Health Biology
76	Fatty Acid Disorders Information for Parents  Overview Fatty acid disorders (also called fatty acid oxidation disorders) are a group of rare, inherited conditions that affect infants from birth. They are caused by enz Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2013-09-05 15:51:36 Rare diseases Fatty acids Metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Mitochondrial trifunctional protein deficiency Health Medicine Biology
77	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
78	Microsoft Word - Disorder list Jan 10 Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:47:40 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Fatty-acid metabolism disorder 3-Methylcrotonyl-CoA carboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Maple syrup urine disease Health Rare diseases Genetic genealogy
79	NEWBORN SCREENING CONFIRMED CASE REPORT PRIMARY PANEL OF 29 DISORDERS DOB[removed] – [removed]Disorder Abbreviation Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:51 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Maple syrup urine disease Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Health Rare diseases Genetic genealogy
80	OFFICE OF NEWBORN SCREENING 2008 CONFIRMED CASE REPORT PRIMARY PANEL OF 28 BLOODSPOT DISORDERS DISORDER ANALYTE Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:54 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Biotinidase deficiency Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy