Rebornne Baby American Baby

Newborns
Learn how to take care of your newborn baby.

State-by-State Newborn Screening
Find out which conditions your state screens newborns for.

Introduction

Newborn screening requirements vary from state to state. Locate your state on the following pages, and find out which tests your newborn is guaranteed to get.

Please note that some states are scheduled to add new screening tests to their roster of requirements. Contact your state's Department of Health for the most recent list of required newborn screening tests.

If you want your child to undergo additional testing, click the "Ordering Additional Tests" link to find out how.

States A-F
Alabama
Galactosemia
Phenylketonuria (PKU)
Congenital Hypothyroidism
Congenital Adrenal Hyperplasia (CAH)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Alaska
Biotinidase Deficiency
Congenital Adrenal Hyperplasia
Galactosemia
Hypothyroidism
Maple Syrup Urine Disease
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies (upon request)

Arizona
Biotinidase Deficiency
Galactosemia
Homocystinuria
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Arkansas
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

California
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Colorado
Biotinidase Deficiency
Congenital Adrenal Hyperplasia (CAH)
Cystic Fibrosis (CF)
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Connecticut
Biotinidase Deficiency
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Homocystinuria
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Delaware
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Florida
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

States G-L
Georgia
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Homocystinuria
Hypothyroidism
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Tyrosinemia

Hawaii
Biotinidase Deficiency
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Idaho
Biotinidase Deficiency
Galactosemia
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)

Illinois
Biotinidase Deficiency
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Indiana
Biotinidase Deficiency
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Homocystinuria
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Iowa
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Hypothyroidism (congenital)
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Kansas
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Kentucky
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Louisiana
Biotinidase Deficiency
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

States M
Maine
Biotinidase Deficiency
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Homocystinuria
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies (upon request)

Maryland
Biotinidase Deficiency
Galactosemia
Homocystinuria
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies
Tyrosinemia Type I & II

Massachusetts
2-Methylbutyryl-CoA Dehydrogenase Deficiency
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (HMG)
3-Ketothiolase Deficiency
3-Methylcrotonyl-CoA Carboxylase Deficiency (3MCC)
Argininosuccinic Aciduria (ASA)
Biotinidase Deficiency
Carnitine Palitoyl Transferase Deficiency Type II (CPT-II) Citrulinemia
Congenital Adrenal Hyperplasia (CAH)
Cystic Fibrosis (CF)
Galactosemia
Glutaric Acidemia II (GA-II) (aka Multiple Acyl-CoA Dehydrogenase Deficiency)
Glutaric Acidemia Type I (GA-I)
Homocystinuria
Hyperammonemia, Hyperornithinemia, Homocitrilinuria Syndrome (HHH)
Hypothyroidism (congenital)
Isovaleric Acidemia (IVA)
Long-Chain Acyl-CoA Dehydrogenase Deficiency (LCAD)
Long-Chain Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD)
Maple Syrup Urine Disease (MSUD)
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
Methylmalonic Aciduria (MMA)
Phenylketonuria (PKU)
Propionic Acidemia (PA)
Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD)
Sickle Cell Disease (SCD) and Hemoglobinopathies
Toxoplasmosis (congenital)
Tyrosinemia Type I & II
Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD)

Michigan
Biotinidase Deficiency
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Minnesota
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Mississippi
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Missouri
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Montana
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)

States N
Nebraska
Biotinidase Deficiency
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Nevada
Biotinidase Deficiency
Galactosemia
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

New Hampshire
Galactosemia
Homocystinuria
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Toxoplasmosis (congenital)

New Jersey
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

New Mexico
Biotinidase Deficiency
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

New York
Biotinidase Deficiency
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Homocystinuria
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

North Carolina
2,4-Dienoyl-CoA Reductase Deficiency
2-Methylbutyryl-CoA Dehydrogenase Deficiency
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (HMG)
3-Ketothiolase Deficiency (aka Mitochondrial Acetoacetyl-Coa Thiolase Deficiency)
3-Methylcrotonyl-CoA Carboxylase Deficiency (3MCC)
3-Methylglutaconyl-CoA Hydratase Deficiency
5-Oxoprolinuria
Argininemia (aka Arginase Deficiency)
Argininosuccinic Aciduria (ASA)
Carnitine Palitoyl Transferase Deficiency Type II (CPT-II)
Carnitine/Acylcarnitine Translocase Deficiency
Citrilinemia
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Glutaric Acidemia II (GA-II) (a.k.a. Multiple Acyl-CoA Dehydrogenase Deficiency)
Glutaric Acidemia Type I (GA-I)
Homocystinuria
Hyperammonemia, Hyperornithinemia, Homocitrilinuria Syndrome (HHH)
Hypermethioninemia
Hypothyroidism (congenital)
Isobutyryl-Coa Dehydrogenase Deficiency
Isovaleric Acidemia (IVA)
Long-Chain Acyl-CoA Dehydrogenase Deficiency (LCAD)
Long-Chain Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD)
Maple Syrup Urine Disease (MSUD)
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
Methylmalonic Aciduria (MMA)
Mitochondrial Acetoacetyl-Coa Thiolase Deficiency
Multiple CoA Carboxylase Deficiency
Nonketotic Hyperglycinemia (NKH)
Phenylketonuria (PKU)
Propionic Acidemia (PA)
Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD)
Sickle Cell Disease (SCD) and Hemoglobinopathies
Thalassemia
Tyrosinemia Type I & II
Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD)

North Dakota
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)

States O-T
Ohio
Galactosemia
Homocystinuria
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Oklahoma
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Oregon
Biotinidase Deficiency
Galactosemia
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Pennsylvania
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Rhode Island
Biotinidase Deficiency
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Homocystinuria
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

South Carolina
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Hypothyroidism (congenital)
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

South Dakota
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)

Tennessee
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Texas
Congenital Adrenal Hyperplasia (CAH)
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

States U-W
Utah
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)

Vermont
Biotinidase Deficiency
Galactosemia
Homocystinuria
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Virginia
Biotinidase Deficiency
Galactosemia
Homocystinuria
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Washington
Congenital Adrenal Hyperplasia (CAH)
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Washington, D.C.
Biotinidase Deficiency
Galactosemia
Homocystinuria
Hypothyroidism (congenital)
Maple Syrup Urine Disease (MSUD)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

West Virginia
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)

Wisconsin
2,4 Dienoyl-CoA Reductase Deficiency
3-Hydroxy-3-Methyglutaryl-CoA Lyase Deficiency (HMG)
3-Methylcrontonyl CoA Carboxylase Deficiency (3-MMC)
Biotinidase Deficiency (BD)
Carnitine Palmitoyltransferase Deficiency Type II (CPT-II)
Congenital Adrenal Hyperplasia (CAH)
Cystic Fibrosis (CF)
Galactosemia
Glutaric Acidemia Type II (GA-II)
Glutaryl CoA Dehydrogenase Deficiency Type I (GA-I)
Hemoglobinopathies
Hypothyroidism
Isovaleryl CoA Dehydrogenase Deficiency (IVA)
Long Chain 3-Hydroxyacyl CoA Dehydrogenase (LCHAD)
Maple Syrup Urine Disease (MSUD) (on selected populations)
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
Methylmalonic Acidemia (MMA)
Mitochondrial Acetoacetyl CoA Thiolase Deficiency (b-KT)
Phenylketonuria (PKU)
Propionyl CoA Carboxylase Deficiency (PA)
Short Chain Acyl-CoA Dehydrogenase Deficiency (SCAD)
Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD)

Wyoming
Biotinidase Deficiency
Cystic Fibrosis (CF)
Galactosemia
Hypothyroidism (congenital)
Phenylketonuria (PKU)
Sickle Cell Disease (SCD) and Hemoglobinopathies

Ordering Additional Tests

If you want your child to undergo additional testing, you can order tests from these organizations:

Neo Gen Screening
866-463-6436
www.neogenscreening.com
43 tests for $24.50

Neo Gen Screening

The Institute of Metabolic Diseases at Baylor University Medical Center
800-422-9567
www.baylorhealth.com/newbornscreening
35 tests for $25

Institute of Metabolic Diseases

NewScreen
800-747-3319
www.newscreentest.com
more than 36 tests for $98.50

NewScreen

Your should know:

The information on this Web site is designed for educational purposes only. It is not intended to be a substitute for informed medical advice or care. You should not use this information to diagnose or treat any health problems or illnesses without consulting your pediatrician or family doctor. Please consult a doctor with any questions or concerns you might have regarding your or your child's condition.