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Carnitine-acylcarnitine translocase
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#	Item
11	Microsoft Word - CAT_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-12-01 02:16:23 Chemistry Carnitine-acylcarnitine translocase deficiency Fatty-acid metabolism disorder Carnitine Translocase Newborn screening Inborn error of lipid metabolism Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
12	NEWBORN SCREENING FACT SHEET CPT-2 Deficiency (Carnitine Palmitoyl Transferase Deficiency, CACT, Type 2) in infancy. Most people do not have symptoms until their teen years or early adulthood. This is called classic form Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:59 Fatty-acid metabolism disorder Hepatology Carnitine Newborn screening Carnitine-acylcarnitine translocase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
13	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
14	` 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
15	Disease Name CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY (CACT) (SOLUTE CARRIER FAMILY 25 (CARNITINE/ACYLCARNITINE TRANSLOCASE), MEMBER 20; CARNITINE-ACYLCARNITINE CARRIER; CACT DEFICIENCY) Fatty acid oxidation defect Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:55 Chemistry Rare diseases Carnitine-acylcarnitine translocase deficiency Translocase Carnitine Hyperammonemia Ketotic hypoglycemia Hypoglycemia Carnitine palmitoyltransferase II deficiency Health Medicine Solute carrier family
16	Microsoft Word - cpt2_ref Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:03 Biology Carnitine palmitoyltransferase I Carnitine CPT2 Fatty-acid metabolism disorder Myoglobinuria Fatty acid metabolism Carnitine-acylcarnitine translocase deficiency Inborn error of lipid metabolism Medicine Hepatology Health
17	Microsoft Word - CPT2_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-12-01 02:35:36 Rare diseases Chemistry Fatty-acid metabolism disorder Fatty acids Carnitine Newborn screening Fatty acid metabolism Carnitine palmitoyltransferase II deficiency Carnitine-acylcarnitine translocase deficiency Health Medicine Hepatology
18	Disorders Detected By Mississippi Genetic Newborn Screening Secondary Conditions Methylmalonic acidemia with homocystinuria Malonic acidemia Isobutyrylglycinuria Add to Reading List Source URL: msdh.ms.gov Language: English - Date: 2012-03-28 12:35:21 Medical genetics Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Propionic acidemia Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Glutaric acidemia type 2 Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy
19	Microsoft Word - CPT2 update, 2011.doc Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2011-05-26 16:26:05 Rare diseases Chemistry Fatty-acid metabolism disorder Fatty acids Carnitine Newborn screening Fatty acid metabolism Carnitine palmitoyltransferase II deficiency Carnitine-acylcarnitine translocase deficiency Health Medicine Hepatology
20	Carnitine/Acylcarnitine Translocase Deficiency (CACT) A fatty acid oxidation disorder What is it? Carnitine/Acylcarnitine Translocase Deficiency (also known as CACT) is an inherited fatty acid oxidation disorder. Patient Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2007-09-13 15:09:34 Fatty-acid metabolism disorder Carnitine-acylcarnitine translocase deficiency Carnitine Newborn screening Health Rare diseases Medicine