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Very long chain fatty acid
Results: 63

#	Item
51	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2009-02-03 16:52:41 Fatty-acid metabolism disorder Mitochondrial trifunctional protein deficiency Newborn screening Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency Health Medicine Rare diseases
52	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2009-02-03 16:51:42 Genetic genealogy Glutaric acidemia type 2 Fatty-acid metabolism disorder Glutaric aciduria type 1 Newborn screening Fatty acid metabolism Propionic acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
53	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
54	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
55	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
56	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
57	Microsoft Word - ALD Info for PCPs_MC_12-18.docx Add to Reading List Source URL: www.wadsworth.org Language: English - Date: 2014-06-24 11:31:21 Peroxisomal disorders Leukodystrophies Adrenal gland disorders Adrenoleukodystrophy ABCD1 Newborn screening Infantile Refsum disease Very long chain fatty acid Genetic counseling Health Medicine Rare diseases
58	Newborn Screening Program Disorders Add to Reading List Source URL: health.utah.gov Language: English - Date: 2013-07-08 12:47:26 Genetic genealogy Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Propionic acidemia Malonyl-CoA decarboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
59	PDF Document Add to Reading List Source URL: bioperoxil.u-bourgogne.fr Language: English - Date: 2014-01-28 10:55:25 Cellular processes Immune system Autophagy Apoptosis Adrenoleukodystrophy Oligodendrocyte Very long chain fatty acid Biology Cell biology Programmed cell death
60	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: chfs.ky.gov Language: English - Date: 2014-08-09 10:55:30 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

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