Disorders screened - Oklahoma State Department of Health

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Disorders screened

Sickle Cell Disease

Family Support Information

Newborn Screening Rules and Regulation

Voice Response System

Historical Statistics

Newborn Screening English Brochure

Newborn Screening Spanish Brochure

National Newborn Screening and Genetics Resource Center

Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children

Genetics Program

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All Oklahoma babies are screened for :

Classic Galactosemia

Parent Information
Provider Information
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Phenylketonuria (PKU)

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MCAD

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Provider Information
Family Support Information

PROP/ MUT

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Provider Information
Family Support Information

Congenital Adrenal Hyperplasia

Parent Information
Provider Information
Family Support Information

Arginine

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CUD

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Family Support Information

GA-I

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Family Support Information

Congenital Hypothyroidism

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Provider Information
Family Support Information

Citrulline

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Provider Information
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SCAD/ GAII

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Provider Information
Family Support Information

3MCC/ HMG/ MCD

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Cystic Fibrosis

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Provider Information
Family Support Information

Leucine (MSUD)

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Provider Information
Family Support Information

VLCAD

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Provider Information
Family Support Information

IVA/ 2MBG

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Sickle Cell Disease

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Provider Information
Family Support Information

Methionine

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CPT2/ CACT

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Provider Information
Family Support Information

MAL

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Biotinidase Deficiency

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Provider Information
Family Support Information

Tyrosine

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Provider Information
Family Support Information

CPT1

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Family Support Information

BKT

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Provider Information
Family Support Information

Newborn Hearing Screening

LCHAD/ TFP

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Family Support Information

IBG

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Provider Information
Family Support Information