Vermont Newborn Screening Program
Phone: 800-660-4427
Phone (alt.): 802-951-5180
FAX: 802-951-1218
Email: AHS.VDHNewbornScreening@vermont.gov
Vermont Newborn Screening Program Website
Total number of conditions screened in this state: 35
3-methylcrotonyl-CoA carboxylase deficiency3-OH 3-CH3 glutaric aciduria
Argininosuccinic acidemia
Beta-ketothiolase deficiency
Biotinidase deficiency
Carnitine uptake defect
Citrullinemia
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Galactosemia
Glutaric acidemia type I
Hb S/beta-thalassemia
Hb S/C disease
Hearing
Homocystinuria
Isovaleric acidemia
Long-chain L-3-OH acyl-CoA dehydrogenase deficiency
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia: cobalamin A, B
Methylmalonic acidemia: mutase deficiency
Mucopolysaccharidosis type I
Multiple carboxylase deficiency
Phenylketonuria
Pompe disease
Propionic acidemia
Severe combined immunodeficiency
Sickle cell anemia
Spinal muscular atrophy
Trifunctional protein deficiency
Tyrosinemia type I
Very long-chain acyl-CoA dehydrogenase deficiency
X-linked adrenoleukodystrophy
Last Reviewed 03/01/2023