| Document Date: 2007-06-25 16:36:39
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City Atlanta / Harthcock / OMIM / Lundy / Oostheim / New York / / Company 3hydroxyacyl-CoA / Eaton / Sim KG / Shimizu / Russell / Lehman / Burlina AB / L 3hydroxyacyl-CoA / McGraw-Hill / Sims HF / Harding CO. / / Facility Arch Dis Child / / IndustryTerm culture media / / MedicalCondition Acute fatty liver / recurrent myoglobinuria / LCHAD deficiency / low platelets syndrome / lipid myopathy / Trifunctional protein deficiency / Long-Chain Acyl CoA Dehydrogenase Deficiency / lethal disorder / CoA DEHYDROGENASE DEFICIENCY / JE / Fatty Acid Oxidation Disorders / myopathy / Bannayan-Riley-Ruvalcaba syndrome / mitochondrial fatty acid oxidation disorders / Acute respiratory distress syndrome / infantile cholestasis / HELLP syndrome / maternal illness / hereditary metabolic chorioretinopathy / Inherited Disease / Lactic acidosis / Hypoparathyroidism / Complete deficiency / related disorders / mitochondrial trifunctional protein deficiency / fetal fatty-acid oxidation disorder / significant maternal hepatic dysfunction / dehydrogenase deficiency / Mild trifunctional protein deficiency / Neonatal lethal mitochondrial trifunctional protein deficiency / Metabolic cardiomyopathies / fatty acid beta-oxidation disorders / deficiency / MS / early-onset liver cirrhosis / liver disease / maternal acute fatty liver / mitochondrial trifunctional protein deficiencies / Cataract / Disorders / / Organization Am Diet Assoc / / Person Van Hoof / Ding J. Mitochondrial / Van Calcar / Arch Pathol Lab Med / Van Maldergem / / Position Jones PM / General / Carpenter / de Klerk HB / van Lith GH / / Product DS / / ProvinceOrState New York / Gillingham / / RadioStation Lund AM / Das AM / / Technology alpha / genotype / / URL www.emedicine.com / /
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Microsoft Word - lchad_ref