Alabama | Newborn Screening

State Newborn Screening Panel

2,4 Dienoyl-CoA reductase deficiency
2-methyl-3-hydroxybutyric aciduria
2-methylbutyrylglycinuria
3-methylcrotonyl-CoA carboxylase deficiency
3-methylglutaconic aciduria
Argininemia
Argininosuccinic acidemia
Benign hyperphenylalaninemia
Beta-ketothiolase deficiency
Biopterin defect in cofactor biosynthesis
Biopterin defect in cofactor regeneration
Biotinidase deficiency
Carnitine acylcarnitine translocase deficiency
Carnitine palmitoyltransferase type I deficiency
Carnitine palmitoyltransferase type II deficiency
Carnitine uptake defect
Citrullinemia
Citrullinemia, type II
Classical galactosemia
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Galactoepimerase deficiency
Galactokinase deficiency
Glutaric acidemia type I
Glutaric acidemia type II
Hb S/beta-thalassemia
Hb S/C disease
Hearing loss
Homocystinuria
Hydroxymethylglutaric Aciduria or HMG-CoA Lyase Deficiency or 3-OH 3-CH3 Glutaric Aciduria
Hypermethioninemia
Isobutyrylglycinuria
Isovaleric acidemia
Long-chain 3-OH acyl-CoA dehydrogenase deficiency
Malonic acidemia
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Medium-chain ketoacyl-CoA thiolase deficiency
Medium/short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency
Methylmalonic acidemia CblA and CblB forms
Methylmalonic acidemia due to mutase deficiency
Methylmalonic acidemia with homocystinuria
Mucopolysaccharidosis type I
Multiple carboxylase deficiency
Phenylketonuria
Pompe disease
Propionic acidemia
Severe combined immunodeficiency
Short-chain acyl-CoA dehydrogenase deficiency
Sickle cell anemia
Spinal muscular atrophy
T-cell related lymphocyte deficiencies
Trifunctional protein deficiency
Tyrosinemia type I
Tyrosinemia, type II
Tyrosinemia, type III
Various other hemoglobinopathies
Very long-chain acyl-CoA dehydrogenase deficiency
X-linked adrenoleukodystrophy

In this state, babies undergo a second screening step when they are around two weeks old. This second screening usually happens in a health care provider’s office. It can help find babies who have conditions that are hard to detect in the first days of life but that still benefit from early treatment or intervention.

Contacts and Support

State Newborn Screening Program

Alabama Newborn Screening Program

Phone: 334-290-3097

Phone (alt.): 866-928-6755

FAX: 334-206-3791

Email: clab@adph.state.al.us

Alabama Newborn Screening Program Website

Early Hearing Detection and Intervention

Alabama EHDI Program

Phone: 334-358-2082

Alabama EHDI Program Website

Additional Resources

For a listing of general support, advocacy, and informational resources for Newborn Screening, visit the Resources page.

Date Last Reviewed:

December 2024