<--- Back to Details
First PageDocument Content
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
Date: 2007-05-01 10:02:30
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)

Add to Reading List

Source URL: health.state.tn.us

Download Document from Source Website

File Size: 22,23 KB

Share Document on Facebook

Similar Documents

Newborn screening / Isovaleric acidemia / Methylmalonic acidemia / Acyl CoA dehydrogenase / Biotinidase deficiency / Galactosemia / Methylmalonic acid / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Guthrie test / Health / Rare diseases / Medicine

Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial

DocID: 14zTU - View Document

Newborn screening / Isovaleric acidemia / Methylmalonic acidemia / Acyl CoA dehydrogenase / Biotinidase deficiency / Galactosemia / Methylmalonic acid / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Guthrie test / Health / Rare diseases / Medicine

Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial

DocID: 11G3r - View Document

Rare diseases / Fatty-acid metabolism disorder / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Glutaric aciduria type 1 / Carnitine / Biotinidase deficiency / Biotin / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Health / Genetic genealogy / Medical genetics

Chart of Metabolic Disorders Screened Table of Disorders Screened by Program Condition Incidence

DocID: Z5KR - View Document

Medical genetics / Newborn screening / Isovaleric acidemia / Methylmalonic acidemia / Propionic acidemia / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Fatty-acid metabolism disorder / Acyl CoA dehydrogenase / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Genetic genealogy

Disorders and Reference Ranges

DocID: KTuv - View Document

Medical genetics / Newborn screening / Isovaleric acidemia / Methylmalonic acidemia / Propionic acidemia / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Fatty-acid metabolism disorder / Acyl CoA dehydrogenase / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Genetic genealogy

Disorders and Reference Ranges

DocID: KToy - View Document