Newborn Screening in Alabama

Alabama Newborn Screening Program
Phone: 866-928-6755
FAX: 334-206-3791

Alabama Newborn Screening Program Website

 

Total number of conditions screened in this state: 31

3-methylcrotonyl-CoA carboxylase deficiency
Argininosuccinic acidemia
Beta-ketothiolase deficiency
Biotinidase deficiency
Carnitine uptake defect
Citrullinemia
Classical galactosemia
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Glutaric acidemia type I
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
Isovaleric acidemia
Long-chain 3-OH acyl-CoA dehydrogenase deficiency
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia CblA and CblB forms
Methylmalonic acidemia due to mutase deficiency
Multiple carboxylase deficiency
Phenylketonuria
Propionic acidemia
Severe combined immunodeficiency
Sickle cell anemia
Trifunctional protein deficiency
Tyrosinemia type I
Very long-chain acyl-CoA dehydrogenase deficiency

 

Last Reviewed 12/01/2022