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Medical genetics / Fatty-acid metabolism disorder / Newborn screening / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine-acylcarnitine translocase deficiency / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Hyperammonemia / Carnitine / Isovaleric acidemia / Health / Rare diseases / Genetic genealogy


STATE OF TENNESSEE DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM
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Document Date: 2011-02-25 12:37:37

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City

HART LANE NASHVILLE / /

Company

mol/L Asa / Methionine (under validation) Ornithine Asa / Argininosuccinic Acid Asa / /

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Facility

Tennessee Department of Health Newborn Screening laboratory / /

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MedicalCondition

Nonketotic Hyperglycinemia Homocystinuria / Citrin Deficiency / diseases / respective disorders / Arginase Deficiency / disorder 3Hydroxyacyl CoA dehydrogenase deficiency / Argininosuccinate Lyase Deficiency / Arginosuccinate Synthetase Deficiency / /

Organization

MADD / DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM / Department of Health Newborn Screening / /

Person

Thomas Childs / Christine D. Mckeever Newborn Screening / Christine McKeever / /

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Position

Manager Date / Division Manager/MSMS Manager / /

Product

C5 / Glycine / C16 / /

ProvinceOrState

Tennessee / /

Technology

Alpha / /

SocialTag