Texas Newborn Screening
Phone: 512-776-3957
Phone (alt.): 800-252-8023 ext. 3957
FAX: 512-776-7450
Email: newborn@dshs.texas.gov
Texas Newborn Screening Website
Texas Newborn Screening Laboratory
Phone: 512-776-7333
Phone (alt.): 888-963-7111 ext. 7333
FAX: 512-776-7157
Email: newbornscreeninglab@dshs.texas.gov
DSHS Newborn Screening Laboratory Website
Total number of conditions screened in this state: 57
2 Methylbutyrylglycinuria2,4 Dienoyl-CoA reductase deficiency
2-methyl-3-hydroxybutyric acidemia
2-methyl-3-hydroxybutyric acidemia
3-hydroxy-3-methylglutaric aciduria
3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency
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 I deficiency
Carnitine palmitoyltransferase type II deficiency
Carnitine uptake defect
Citrullinemia, type I
Citrullinemia, type II
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Galactosemia
Glutaric acidemia type I
Glutaric acidemia type II
Hearing
Homocystinuria
Hypermethioninemia
Isobutyrylglycinuria
Isovaleric acidemia
Long chain L-3-hydroxyacyl-CoA dehydrogenase deficiency
Malonic acidemia
Maple syrup urine disease
Medium-chain ketoacyl-CoA thiolase deficiency
Methylmalonic acidemia (Cbl A and Cbl B forms)
Methylmalonic acidemia (mutase deficiency form)
Methylmalonic acidemia with homocystinuria
Multiple carboxylase deficiency
Phenylketonuria
Propionic acidemia
S Beta-thalassemia
S,C disease
S,S (Sickle cell anemia)
Severe combined immunodeficiencies
Short-chain acyl-CoA dehydrogenase deficiency
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
Last Reviewed 03/01/2023
