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Fatty acids / Metabolism / Mitochondrial trifunctional protein / Proteins / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Fatty-acid metabolism disorder / Hepatology / Hydroxyacyl-Coenzyme A dehydrogenase / HADHA / Biology / Health / Chemistry


Disease Name LONG-CHAIN HYDROXYACYL-CoA DEHYDROGENASE (LCHAD) (LCHAD; MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFECT; LONG-CHAIN HYDROXYACYL-CoA DEHYDROGENASE; LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY) Fatty aci
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Document Date: 2007-06-25 16:36:38


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City

Malvern / /

Company

Screening Foundation Inc / FOD (Fatty Oxidation Disorder) Family Support Group / /

Country

Finland / /

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Facility

National Library of Medicine Genetics Home Reference Mitochondrial / Oregon Health Services University / Climb Building / National Library of Medicine Genetics Home Reference Long-chain / /

IndustryTerm

carrier frequency / oil / /

MedicalCondition

acute fatty liver / Inherited Metabolic Diseases / HELLP / trifunctional protein deficiency / Cardiomyopathy / CoA DEHYDROGENASE DEFICIENCY / chronic progression / liver failure / email@savebabies.org Trifunctional Protein Deficiency FOD / chronic / non-specific symptoms / progressive disease / Maternal pregnancy complications / unrecognized hypoglycemia / thrombocytopenia / retinal degeneration / Hypoparathyroidism / progressive peripheral neuropathy / dehydrogenase deficiency / myoglobinuria / hypotonia / MS / hypoglycemia / anemia / Fatty Oxidation Disorder / /

Organization

Oregon Health Services University in Portland / Babies Through Screening Foundation / /

Person

Sara Copeland / Judith Tuerck / Lorinda Paradise / /

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ProvinceOrState

ARDS / Oregon / Iowa / Pennsylvania / /

PublishedMedium

Natural History / /

URL

www.fodsupport.org / http /

SocialTag