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Medical genetics / Newborn screening / Methylmalonic acidemia / Glutaric aciduria type 1 / Propionic acidemia / Isovaleric acidemia / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Glutaric acidemia type 2 / Carnitine-acylcarnitine translocase deficiency / Health / Rare diseases / Genetic genealogy


Disorders Detected By Mississippi Genetic Newborn Screening Secondary Conditions Methylmalonic acidemia with homocystinuria Malonic acidemia Isobutyrylglycinuria
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Document Date: 2012-03-28 12:35:21

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City

Jackson / /

Company

ketoacyl-CoA / acyl-CoA / /

MedicalCondition

S disease / aciduria Citrullinemia / mental retardation / II Tyrosinemia / disease / acylcarnitine translocase deficiency Argininemia Citrullinemia / cofactor regeneration Tyrosinemia / phenylketonuria Tyrosinemia / Beta-thalassemia S / Sickle cell anemia / cobalamin disorders / CoA carboxylase deficiency / specific disorders / disorders / different genetic disorders / genetic disorders / /

Organization

MISSISSIPPI STATE DEPARTMENT OF HEALTH / Division of Genetic Services Post office Box / /

/

Position

physician / /

ProvinceOrState

Mississippi / /

URL

www.HealthyMS.com / /

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