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Genetic genealogy / Newborn screening / Methylmalonic acidemia / Propionic acidemia / Medium-chain acyl-coenzyme A dehydrogenase deficiency / 2-Methylbutyryl-CoA dehydrogenase deficiency / Isovaleric acidemia / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Glutaric aciduria type 1 / Health / Rare diseases / Medicine


Newborn Screening Brochure
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Document Date: 2011-10-11 08:14:49

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City

Albany / /

Company

acyl-CoA / hydroxyacyl-CoA / ketoacyl-CoA / /

Currency

MGA / /

Facility

Newborn Screening Program Wadsworth Center / /

MedicalCondition

HIV infection / lyase deficiency / specific disorder / mental retardation / trifunctional protein deficiency / CoA dehydrogenase deficiency / HIV / Hyperphenylalaninemia (HyperPhe) Tyrosinemia / particular disorder / hypothyroidism / beta-ketothiolase deficiency / Sickle cell anemia / Argininemia / Congenital hypothyroidism / Citrullinemia / Methylmalonyl-CoA mutase deficiency / dehydrogenase deficiency / disorder / CoA reductase deficiency / PKU / AIDS / Carnitine-acylcarnitine translocase deficiency / infection / acetoacetyl-CoA thiolase deficiency / deficiency / Phenylketonuria / Multiple carboxylase deficiency / Biotinidase deficiency / Cystic Fibrosis / several rare disorders / CoA carboxylase deficiency / Isobutyryl-CoA dehydrogenase deficiency / Hb SS disease / serious illness / Maple syrup urine disease / disorders / Homocystinuria / /

MedicalTreatment

counseling / /

Organization

Department of State / New York State Department / MADD / Department of Health / /

/

Position

Hb / Hb SC disease Hb / nurse / specialist / /

ProvinceOrState

New York / New / /

Technology

antibodies / CAT / /

URL

www.wadsworth.org/newborn/index.htm / www.wadsworth.org / /

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