Back to Results
First PageMeta Content
Genetic genealogy / Newborn screening / Carnitine / Fatty-acid metabolism disorder / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Glutaric aciduria type 1 / Methylmalonic acidemia / Glutaric acidemia type 2 / Acyl CoA dehydrogenase / Health / Rare diseases / Medicine


Delaware Division of Public Health Newborn Screening Program Disorder Name & Abbreviation Analyte / Marker Endocrine Disorder
Add to Reading List

Document Date: 2012-07-26 14:33:28

Open Document

File Size: 108,84 KB

Share Result on Facebook

Company

3M / /

MedicalCondition

Methylcrotonyl-CoA Carboxylase Deficiency / Acidemia (MMA) Multiple Carboxylase Deficiency / Carnitine/Acylcarnitine Translocase Deficiency / Trifunctional Protein Deficiency / Congenital Adrenal Hyperplasia / CoA Lyase Deficiency / Carnitine Uptake Deficiency / SCID / Beta-Ketothiolase Deficiency / Multiple Acyl-CoA Dehydrogenase Deficiency / III (TYR) Argininemia / Hyperphenylalanemia (HPHE) Maple Syrup Urine Disease / Citrullinemia / mol/L mol/L mol/L Short-Chain Acyl-CoA Dehydrogenase Deficiency / mol/L mol/L mol/L Fatty Acid Oxidation Disorders Other Genetic Disorders Galactosemia Hemoglobinopathies Biotinidase Deficiency Cystic Fibrosis / II Deficiency / Argininosuccinate Lyase Deficiency / Hypermethioninemia (HMET) Tyrosinemia / Homocystinuria / /

Organization

MADD / Delaware Division of Public Health Newborn Screening Program Disorder Name & Abbreviation Analyte / /

Position

days Units U/gm Hb / /

Technology

ASL / html / CAT / /

URL

http /

SocialTag