Tennessee

Tennessee Newborn Screening
Phone: 615-532-8462
Phone (alt.): 855-202-1357
FAX: 615-532-8555
Email: nbs.health@tn.gov

Tennessee Newborn Screening Website

Tennessee Newborn Screening Laboratory
Phone: 615-262-6353
FAX: 615-262-6447
Email: labnbs.health@tn.gov

Tennessee Newborn Screening Laboratory Website

Tennessee Newborn Screening Follow-up
Phone: 615-532-8462
Phone (alt.): 855-202-1357
FAX: 615-532-8555
Email: nbs.health@tn.gov

 

Total number of conditions screened in this state: 68

2 methyl 3 hydroxybutyric aciduria
2,4 Dienyl CoA reductase deficiency
2-methylbutyryl-CoA dehydrogenase deficiency
3 hydroxy 3 methylglutaric aciduria
3 methyl crotonyl CoA carboxylase deficiency
3 methylglutaconyl CoA hydratase deficiency
Argininemia (Arginase deficiency)
Argininosuccinic aciduria
Benign hyperphenylalaninemia (due to biopterin defect in co-factor biosynthesis)
Benign hyperphenylalaninemia (due to biopterin defect in co-factor regeneration)
Benign hyperphenylalaninemia (due to phenylalanine hydroxylase deficiency, GTP cyclohydrolase I deficiency, pterin-4-alpha carbinolamine dehydratase deficiency, and 6-pyruboyltetahydropterin synthase deficiency)
Biotinidase deficiency
Carbamoyl phosphate synthetase I deficiency
Carnitine acylcarnitine translocase deficiency
Carnitine palmitoyltransferase type I deficiency
Carnitine palmitoyltransferase type II deficiency
Carnitine uptake defect
Carnitine uptake defect/transport defect
Citrullinemia type I (Argininosuccinate synthetase deficiency)
Citrullinemia type II
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart defect
Cystic fibrosis
Fabry disease
Galactokinase deficiency
Galactose epimerase deficiency
Galactosemia
Gaucher disease
Glutaric acidemia type I
Glutaric acidemia type II
Glygogen Storage Disorder Type II (Pompe)
Hearing loss
Hemoglobin SC disease
Homocystinuria or variant forms of hypermethioninemia
Hypermethioninemia
Hyperornithinemia
Isobutyrylglycinuria
Isovaleric acidemia
Krabbe disease
Long chain L-3-hydroxyacyl-CoA dehydrogenase deficiency
Malonic acidemia
Maple syrup urine disease (type IA, IB, II)
Medium chain acylCoA dehydrogenase deficiency
Medium/short chain 3 hydroxyacyl CoA dehydrogenase deficiency
Methylmalonic acidemia (cobalamin disorders)
Methylmalonic acidemia with homocystinuria
Methylmalonyl-CoA mutase deficiency
Mucopolysaccharidosis type I
Multiple CoA carboxylase deficiency
Nonketotic hyperglycinemia
Ornithine transcarbamylase deficiency
Other Variant hemoglobinopathies
Phenylketonuria
Propionic acidemia
Severe combined immunodeficiency
Short chain acylCoA dehydrogenase deficiency
Sickle beta thalassemia
Sickle cell anemia
Spinal muscular atrophy due to homozygous deletion of exon 7 in SMN1
T-cell related lymphocyte deficiencies
Trifunctional protein deficiency
Tyrosinemia type I (Hepatorenal)
Tyrosinemia type II
Tyrosinemia type III
Very long chain acylCoA dehydrogenase deficiency
X-linked adrenyleukodystrophy
β ketothiolase deficiency

 

Last Reviewed 03/01/2023