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Medicine / Coenzymes / Fatty acids / Inborn error of lipid metabolism / Fatty-acid metabolism disorder / Fatty acid metabolism / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Carnitine / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Biology / Chemistry / Metabolism


PRENATAL DIAGNOSIS Prenat Diagn 2001; 21: 52±54. INVITED COMMENTARY: CURRENT ISSUES IN OBSTETRICS AND GENETICS
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Document Date: 2012-05-31 13:41:15

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Rochester / RINALDO ET / /

Company

LCHAD / MCKAT / SCHAD / CVS / SCAD / VLCAD / acyl-CoA / John Wiley & Sons Ltd. / MCAD / D. Matern Biochemical Genetics Laboratory / Biochemical Genetics Laboratory / /

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Facility

Mayo Clinic / Laboratory Medicine / /

IndustryTerm

energy production / splice site / higher energy consumption / gas chromatography/mass spectrometry / energy / /

MedicalCondition

FATMO disorders / acute fatty liver / inherited metabolic disorders / HELLP / cardiomyopathy / metabolic diseases / AC Disorders / FATMO disorder / HELLP syndrome / pregnancy Disorders / skeletal myopathy / fulminant liver disease / disorder / maternal liver disease / treatable disorder / metabolic disorders / illness / hypoketotic hypoglycemia / glutaric aciduria type II / disorders / fetal fatty acid oxidation disorder / /

Person

Roe / /

ProvinceOrState

Minnesota / /

Technology

gas chromatography / /

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