Nevada Newborn Screening Program
Phone: 702-289-4578
FAX: 866-678-5589
Email: ogentscheff@med.unr.edu
Nevada Newborn Screening Program Website
Total number of conditions screened in this state: 46
2-methyl-3-hydroxybutyryl CoA dehydrogenase deficiency2-methylbutyryl CoA dehydrogenase deficiency
3-methylcrotonyl CoA carboxylase deficiency
3-methylglutaconyl CoA hydratase deficiency
Argininemia
Argininosuccinic aciduria
Beta-ketothiolase deficiency
Biotinidase deficiency
Carnitine palmitoyltransferase I deficiency
Carnitine palmitoyltransferase II deficiency
Carnitine uptake defect
Citrullinemia
Classic galactosemia
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Galactoepimerase deficiency
Galactokinase deficiency
Glutaric acidemia type 1
Glutaric acidemia, type II
Hemoglobinopathies
Homocystinuria
Hydroxymethylglutaric aciduria
Isobutyryl CoA dehydrogenase deficiency
Isovaleric acidemia
Long chain 3 hydroxyacyl‑CoA dehydrogenase deficiency
Malonic aciduria
Maple syrup urine disease
Medium chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia, CBl A and B forms
Methylmalonic acidemia, mutase deficiency form
Multiple carboxylase deficiency
Newborn hearing loss
Phenylketonuria
Propionic acidemia
S,C disease
S,S disease (sickle cell anemia)
Severe combined immunodeficiency
Short chain acyl-CoA dehydrogenase deficiency
Sickle beta thalassemia
Sickle cell trait
Trifunctional protein deficiency
Tyrosinemia, type I
Tyrosinemia, type II
Very long chain acyl-CoA dehydrogenase deficiency
Last Reviewed 03/01/2023
