Newborn Screening in Montana

Montana’s Newborn Screening Program
Phone: 406-444-0930
Email: cfortune@mt.gov

Montana’s Newborn Screening Program Website

 

Total number of conditions screened in this state: 33

3-hydroxy-3-methylglutaryl-CoA lyase deficiency
3-methylcrotonyl-CoA carboxylase deficiency
Argininosuccinic acidemia
Biotinidase 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
Hearing loss
Hemoglobin S/β-thalassemia
Hemoglobin SC disease
Homocystinuria
Isovaleric acidemia
Long-chain L-3 hydroxyacyl-CoA dehydrogenase deficiency
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia (cobalamin disorders)
Methylmalonic acidemia (methylmalonyl-CoA mutase)
Multiple carboxylase deficiency
Phenylketonuria
Propionic acidemia
Severe combined immunodeficiency
Sickle cell anemia
Spinal muscular atrophy
Trifunctional protein deficiency
Tyrosinemia type I
Very long-chain acyl-CoA dehydrogenase deficiency
β-ketothiolase deficiency

 

Last Reviewed 03/01/2023