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Fatty acids / Fatty-acid metabolism disorder / Rare diseases / Fatty acid metabolism / Carnitine / Acyl CoA dehydrogenase / Medical genetics / Inborn error of lipid metabolism / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Medicine / Health / Very long-chain acyl-coenzyme A dehydrogenase deficiency


Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency (metabolic condition: fatty acid oxidation disorder) Also known as: • acyl-CoA dehydrogenase very long chain deficiency • very long-chain acyl coenzyme A de
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Document Date: 2013-09-16 18:37:04

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Company

acyl-CoA / 2888 Shaganappi Trail N.W. Calgary AB / St. N.W. Edmonton AB / /

Facility

Children’s Hospital / Edmonton Medical Genetics Clinic / Inherited Metabolic Disorders Clinic / Medical Sciences Building / /

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IndustryTerm

cellular energy deficiency / long chain / energy / /

MedicalCondition

fatty acid oxidation disorder / VLCAD deficiency / very long chain deficiency / fatty acid oxidation disorders / metabolic diseases / seizures / coma / muscle weakness / Dehydrogenase (VLCAD) Deficiency / minor illness / lethargy / vomiting / fatigue / common illness / disorder / diarrhea / hypotonia / illness / hypoglycemia / /

MedicalTreatment

counselling / /

Organization

Inherited Metabolic Disorders Clinic Alberta Children’s Hospital / /

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Position

genetic metabolic specialist / /

URL

www.albertahealthservices.ca/newbornscreening.asp / /

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