South Carolina Newborn Screening
Phone: 803-898-3192
Phone (alt.): 803-898-0619
FAX: 803-898-0337
Email: spellsty@dhec.sc.gov
South Carolina Newborn Screening Website
Total number of conditions screened in this state: 58
2-methyl-3-OH-butyric aciduria2-methylbutyryl coA dehydrogenase deficiency
3-methyl-3-OH-glutaryl coA lyase deficiency
3-methyl-glutaconyl coA hydratase deficiency
3-methylcrotonyl coA carboxylase deficiency
Argininosuccinic aciduria
Benign hyperphenylalaninemia
Biotinidase deficiency
Carnitine palmitoyl transferase I deficiency
Carnitine palmitoyl transferase II deficiency
Carnitine uptake/transport deficiency
Carnitine/acylcarnitine translocase deficiency
Citrullinemia I
Citrullinemia II
Congenital adrenal hyperplasia
Critical congenital heart disease
Cystic fibrosis
Defect of biopterin cofactor biosynthesis
Defect of biopterin cofactor regeneration
Dienoyl coA reductase deficiency
Galactokinase deficiency
Galactose epimerase deficiency
Galactosemia
Glutaric aciduria I
Hearing loss
Homocystinuria
Hypermethioninemia
Isobutyryl glycinuria
Isovaleric acidemia
Long chain 3-OH coA dehydrogenase deficiency
Malonic acidemia
Maple syrup urine disease
Medium chain acyl coA dehydrogenase deficiency
Medium chain ketoacyl coA thiolase deficiency
Medium/short-chain 3-OH acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia- CoA mutase deficiency
Methylmalonic acidemia- Other
Methylmalonic acidemia-Vit B 12 disorders
Mucopolysaccharidosis type I
Multiple acyl coA dehydrogenase deficiency (glutaric aciduria II)
Multiple carboxylase deficiency aka holocarboxylase synthetase deficiency
Phenylketonuria
Pompe disease
Primary congenital hypothyroidism
Propionic acidemia
Severe combined immunodeficiency and related disorders
Short-chain acyl Co-A dehydrogenase deficiency
Sickle C disease
Sickle cell disease
Sickle β thalassemia
Spinal muscular atrophy
Trifunctional protein deficiency
Tyrosinemia I
Tyrosinemia II
Tyrosinemia III
Variant hemoglobinopathy disorders and traits (including sickle cell trait)
Very long chain acyl coA dehydrogenase deficiency
β-ketothiolase deficiency
Last Reviewed 03/01/2023
