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Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Fatty acids / Fatty-acid metabolism disorder / Acute fatty liver of pregnancy / Hepatology / Newborn screening / Fatty acid metabolism / Mitochondrial trifunctional protein / Health / Medicine / Rare diseases


Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
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Document Date: 2009-02-03 16:51:53

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File Size: 19,25 KB

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Company

FOD (Fatty Oxidation Disorder) Family Support Group / /

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IndustryTerm

elevated chemicals / food / energy / /

MedicalCondition

HELLP syndrome / acute fatty liver / fatty acid oxidation disorders / inherited fatty acid oxidation disorder / Long Chain Hydroxyacyl-CoA Dehydrogenase Deficiency / rare fatty acid oxidation disorders / cardiac arrest / autosomal recessive disorder / metabolic disorders / coma / hypoglycemia / Fatty Oxidation Disorder / muscle weakness / /

Movie

What is it? / /

Organization

United Mitochondrial Disease Foundation / Save Babies Through Screening Foundation / /

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Position

physician / care physician / /

ProvinceOrState

Pennsylvania / /

URL

http /

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