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Fatty acids / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Fatty-acid metabolism disorder / Mitochondrial trifunctional protein deficiency / 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Hydroxyacyl-Coenzyme A dehydrogenase / Fatty acid metabolism / Mitochondrial trifunctional protein / ACADL / Health / Chemistry / Medicine


Long Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency (metabolic condition: fatty acid oxidation disorder) Also known as: • long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency • long-chain 3-OH acy
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Document Date: 2013-09-16 18:33:43

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Company

2888 Shaganappi Trail N.W. Calgary AB / St. N.W. Edmonton AB / /

Facility

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

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IndustryTerm

cellular energy deficiency / long chain / energy / /

MedicalCondition

fatty acid oxidation disorder / LCHAD deficiency / acyl-CoA dehydrogenase deficiency / cardiomyopathy / fatty acid oxidation disorders / metabolic diseases / seizures / coma / minor illness / lethargy / vomiting / common illness / dehydrogenase deficiency / diarrhea / hypotonia / deficiency / illness / liver disease / hypoketotic hypoglycemia / Dehydrogenase (LCHAD) Deficiency / /

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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