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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


Medium chain acyl-CoA Dehydrogenase Deficiency (MCADD)
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Document Date: 2007-05-01 10:02:30

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File Size: 22,23 KB

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Company

FAOD / acyl-CoA Dehydrogenase Deficiency / Acyl / /

Event

Product Issues / /

IndustryTerm

food intake / oil / long chain / food / energy / /

MedicalCondition

hepatic encephalopathy seizures / fatty acid oxidation disorder / fatty acid oxidative disorders / acyl-CoA Dehydrogenase Deficiency / Hypertrophic cardiomyopathy / Trifunctional Protein deficiency / cardiomyopathy / Fatty acid oxidation disorders / suspected disorder / myopathy / seizures / liver failure / metabolic acidosis / coma / specific disorders / intercurrent infections / organic acid disorder / hepatic encephalopathy / Dienoyl CoA Reductase deficiency / lethargy / rhabdomyolysis / vomiting / lactic acidosis / Carnitine/Acylcarnitine Translocase deficiency / rare autosomal recessive disorder / attention deficit hyperactive disorder / rare disorders / infection / Carnitine deficiency / autosomal recessive disorder / chronic weakness / hypoglycemia / hypoketotic hypoglycemia / disorders / /

Organization

Carnitine administration / Vanderbilt University School of Medicine Definition / /

Person

John A Phillips / Marilee Weingartner / /

Product

renal excretion / /

Technology

diagnostic tests / CAT / /

SocialTag