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Glutaric acid
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21	Microsoft Word - CA_nbsdisorders07_09_08.doc Add to Reading List Source URL: genes-r-us.uthscsa.edu Language: English - Date: 2012-01-31 16:28:55 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Methylmalonyl-CoA mutase Methylmalonic acid Thiolase Health Rare diseases Genetic genealogy
22	Microsoft Word - Chart_of_Table_of_Metabolic_Disorders_rev.doc Add to Reading List Source URL: health.hawaii.gov Language: English - Date: 2013-05-30 20:03:03 Rare diseases Fatty-acid metabolism disorder Glutaric aciduria type 1 Very long-chain acyl-coenzyme A dehydrogenase deficiency Carnitine Biotinidase deficiency Biotin Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Genetic genealogy
23	NEWBORN SCREENING FACT SHEET GA-1 (Glutaric Acidemia, Type 1) What is it? GA-1 stands for glutaric acidemia, type 1. It is one type of organic acid disorder. People Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:55 Rare diseases Pediatrics Essential amino acids Ketogenic amino acids Proteinogenic amino acids Glutaric aciduria type 1 Newborn screening Phenylketonuria Glutaryl-CoA dehydrogenase Health Medicine Biology
24	NEWBORN SCREENING FACT SHEET GA-2 (Glutaric Acidemia, Type 2) If GA-2 is not treated, what problems occur? GA-2 can cause bouts of illness called metabolic crises. Some of the first symptoms of Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:56 Diabetes Rare diseases Glutaric aciduria type 1 Hypoglycemia Newborn screening Fatty-acid metabolism disorder Acidosis Blood sugar Glutaric acidemia type 2 Health Medicine Genetic genealogy
25	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
26	Disease Name GLUTARIC ACIDEMIA TYPE II (GA II) (GLUTARIC ACIDURIA TYPE II; GA II; ETHYLMALONIC-ADIPIC ACIDURIA; ELECTRON TRANSFER FLAVOPROTEIN DEHYDROGENASE DEFICIENCY; ETF/ETF QO DEFICIENCY) Classification: Fatty acid o Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:18 Glutaric acidemia type 2 Pediatrics Newborn screening Hepatology Glutaric aciduria type 1 Organic acidemia Systemic primary carnitine deficiency Hypoglycemia Electron-transferring-flavoprotein dehydrogenase Health Medicine Rare diseases
27	Glutaric Acidemia, Type 1 (GA1) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel 24 to 36 hours after birth. The blood is tested for rare, hidden disorde Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 21:12:30 Chemistry GA1 Newborn screening Screening Lysine Glutaric acid Health Medicine Glutaric aciduria type 1
28	Robust Summaries & Test Plan: cyclohexane, oxidezed, aq. ext.; Revised Test Plan Add to Reading List Source URL: www.epa.gov Language: English - Date: 2010-03-22 11:01:14 Adipic acid Monomers Carboxylic acid Oxalic acid Acetic acid 1 6-Hexanediol Lipid Glutaric acid Acid Chemistry Dicarboxylic acids Household chemicals
29	Robust Summaries & Test Plan: cyclohexane, oxidezed, aq. ext.; Test Plan Add to Reading List Source URL: www.epa.gov Language: English - Date: 2006-08-04 12:10:04 Glutaric acid Carboxylic acid Acetic acid Oxalic acid Median lethal dose Acids in wine Nitric acid Toxicity Succinic acid Chemistry Dicarboxylic acids Adipic acid
30	Microsoft Word[removed]Condition list.doc Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2014-09-16 08:12:01 Medical genetics Hyperammonemia Glutaric aciduria type 1 Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Propionic acidemia Fatty-acid metabolism disorder Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy

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