Wyoming Newborn Screening Program
Phone: 307-777-6297
FAX: 307-777-7215
Wyoming Newborn Screening Program Website
Total number of conditions screened in this state: 46
3-hydroxy-3-methylglutaryl-CoA lyase deficiency3-methylcrotonyl-CoA carboxylase deficiency
3-methylglutaconic aciduria
Arginase deficiency
Argininosuccinic acidemia
Beta-ketothiolase deficiency
Biotinidase
Carnitine acylcarnitine translocase deficiency
Carnitine palmitoyltransferase deficiency 1a
Carnitine palmitoyltransferase 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 loss
Hemoglobin SC disease
Homocystinuria
Hypermethioninemia
Isovaleric acidemia
Long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency
Malonic acidemia
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia (cobalamin disorders, vitamin B12 disorders)
Methylmalonic acidemia (methylmalonyl-CoA mutase)
Methylmalonic acidemia with homocystinuria
Multiple carboxylase deficiency
Phenylketonuria
Pompe
Propionic acidemia
Severe combined immunodeficiency
Short-chain acyl-CoA dehydrogenase deficiency
Sickle cell anemia
Spinal muscular atrophy
Trifunctional protein deficiency
Tyrosinemia, type I
Tyrosinemia, type II
Tyrosinemia, type III
Very long-chain acyl-CoA dehydrogenase deficiency
X-linked adrenoleukodystrophy
Last Reviewed 03/01/2023
