<--- Back to Details
First PageDocument Content
Fatty acids / Metabolism / Coenzymes / Rare diseases / Fatty-acid metabolism disorder / Beta oxidation / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / ACADVL / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Biology / Chemistry / Biochemistry
Date: 2007-06-25 16:38:01
Fatty acids
Metabolism
Coenzymes
Rare diseases
Fatty-acid metabolism disorder
Beta oxidation
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
ACADVL
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Biology
Chemistry
Biochemistry

Microsoft Word - vlcad_ref

Add to Reading List

Source URL: www.idph.state.ia.us

Download Document from Source Website

File Size: 35,93 KB

Share Document on Facebook

Similar Documents

Rare diseases / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Fatty-acid metabolism disorder / Metabolism / ACADVL / Newborn screening / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Hypoglycemia / Carnitine / Health / Medicine / Chemistry

Disease Name VERY LONG-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY (VLCADD) (VLCAD DEFICIENCY) Fatty acid oxidation disorder Classification: Inheritance:

DocID: yv5l - View Document

Fatty acids / Metabolism / Coenzymes / Rare diseases / Fatty-acid metabolism disorder / Beta oxidation / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / ACADVL / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Biology / Chemistry / Biochemistry

Microsoft Word - vlcad_ref

DocID: xwwy - View Document

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

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

DocID: sPXM - View Document

Medical genetics / Newborn screening / Inborn error of lipid metabolism / ACADVL / Health / Rare diseases / Genetic genealogy

New Hampshire Newborn Screening Panel As of July 1, 2010 Acronym Argininosuccinic Aciduria ASA Argininemia ARG

DocID: seXe - View Document

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

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

DocID: iVJA - View Document