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Carnitine-acylcarnitine translocase deficiency
Results: 41

#	Item
21	Carnitine Palmitoyl Transferase 2 Deficiency (CPT2) / Carnitine Acylcarnitine Translocase Deficiency (CACT) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s h Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 21:09:48 Rare diseases Hepatology CPT2 Carnitine palmitoyltransferase II deficiency Solute carrier family Carnitine-acylcarnitine translocase deficiency Carnitine O-palmitoyltransferase Carnitine Newborn screening Health Medicine Biology
22	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
23	Microsoft Word - RCPU Newborn Screening.doc Add to Reading List Source URL: www.peds.ufl.edu Language: English - Date: 2007-12-31 10:54:00 Rare diseases Newborn screening Inborn error of lipid metabolism Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Inborn error of metabolism Medical genetics Carnitine-acylcarnitine translocase deficiency Isovaleric acidemia Health Medicine Biology
24	Microsoft Word - mso31.doc Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2006-09-11 10:19:50 Rare diseases Systemic primary carnitine deficiency Fatty-acid metabolism disorder Carnitine Newborn screening Fatty acid metabolism Cud Carnitine palmitoyltransferase I deficiency Carnitine-acylcarnitine translocase deficiency Health Medicine Hepatology
25	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
26	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
27	Disease Name Carnitine uptake deficiency Alternate name(s) Acronym Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 04:12:31 Systemic primary carnitine deficiency Dietary supplements Quaternary ammonium compounds Carnitine Fatty-acid metabolism disorder Medical genetics Cardiomyopathy Carnitine-acylcarnitine translocase Medicine Health Hepatology
28	PARENT FACT SHEET DISORDER Carnitine uptake defect (CUD) CAUSE CUD occurs when an enzyme, called “carnitine transporter” (CT), is either missing or not working properly. Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 03:22:03 Chemistry Dietary supplements Quaternary ammonium compounds Carnitine Systemic primary carnitine deficiency Hypoglycemia Carnitine palmitoyltransferase I deficiency Carnitine-acylcarnitine translocase deficiency Medicine Health Hepatology
29	STATE OF TENNESSEE DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM Add to Reading List Source URL: health.tn.gov Language: English - Date: 2011-02-25 12:37:37 Medical genetics Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hyperammonemia Carnitine Isovaleric acidemia Health Rare diseases Genetic genealogy
30	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