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Medical genetics / Newborn screening / Propionic acidemia / Fatty-acid metabolism disorder / 2-Methylbutyryl-CoA dehydrogenase deficiency / Biotinidase deficiency / Isovaleric acidemia / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Methylmalonic acidemia / Health / Rare diseases / Genetic genealogy


State of Illinois Rod R. Blagojevich, Governor Department of Public Health Eric E. Whitaker, M.D., M.P.H., Director Newborn Metabolic
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Document Date: 2007-07-24 10:41:11


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File Size: 1,16 MB

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City

Chicago / Springfield / /

Company

Newborn Screening Laboratory / /

Event

Product Issues / /

Facility

Laboratory Techniques / IDPH's Center / Laboratory Techniques Prior to July / IDPH laboratory / Newborn Screening Laboratory / /

IndustryTerm

energy / chemical processes / appropriate follow-up services / /

MedicalCondition

Congenital Primary Hypothyroidism / Methylcrotonyl-CoA Carboxylase Deficiency / Profound Biotinidase Deficiency / IBD / Short Chain Acyl-CoA Dehydrogenase Deficiency / Congenital Adrenal Hyperplasia / Organic Acid Disorders / JE / Fatty Acid Oxidation Disorders / Urea Cycle Disorders / diagnosed metabolic disorders / Untreated Homocystinuria / treatable disorders / Untreated Biotinidase Deficiency / Galactosemia / newly screened disorders / each metabolic disorder / Tyrosinemia / disorder / Amino Acid Disorders / Trifbnctional Protein Deficiency / CoALyase Deficiency / Long Chain Hydroxyacyl-CoA Dehydrogenase Deficiency / Classical Phenylketonuria / ILLINOIS NEWBORNS Biotinidase Deficiency / selected metabolic disorder / Phenylketonuria / Medium Chain Acyl-CoA Dehydrogenase Deficiency / metabolic disorders / cystic fibrosis / illness / Other Hemoglobinopathies / specific metabolic disorder / Homocystinuria / Methylglutaryl-CoALyase Deficiency / CarnitineIAcylcarnitine Translocase Deficiency / mental retardation / disease / Classical Galactosemia / hypothyroidism / Beta-ketothiolase Deficiency / Trihnctional Protein Deficiency / Classical Congenital Adrenal Hyperplasia / congenital metabolic disorders / Congenital Hypothyroidism / MediumlShort Chain Acyl-CoA Dehydrogenase Deficiency / Very Long Chain Acyl-CoA Dehydrogenase Deficiency / CarnitineIAcylcarnitineTranslocase Deficiency / newborn metabolic disorder / Methylbutyryl-CoA Dehydrogenase Deficiency / treatable metabolic disorders / INTRODUCTION Metabolic Disorders Metabolic disorders / diseases / each screened metabolic disorder / Dehydrogenase Deficiency / PKU / Sickle Cell Disease / Multiple (CoA) Carboxylase Deficiency / inborn errors of metabolism / CoADehydrogenase Deficiency / Additional metabolic disorders / certain metabolic diseases / biotinidase deficiency / metabolic disorder / Isobutyryl-CoA Dehydrogenase Deficiency / selected metabolic disorders / Maple Syrup Urine Disease / disorders / /

MedicalTreatment

surgery / /

Organization

Department of Public Health Eric E. Whitaker / Pediatrics Newborn Screening Task Force / Illinois Department of Public Health / American Academy / IDPH's Center for Health Statistics / U.S. Centers for Disease Control and Prevention / /

Person

David Jinks / Charlene Collin / Newborn Metabolic Screening / Newborn Metabolic / Eric E. Whitaker / Rod R. Blagojevich / /

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Position

Governor / Director / /

Product

gene / use / /

ProvinceOrState

Illinois / /

Technology

Information Technology / /

URL

http /

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