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Vermont

State Newborn Screening Panel

Total number of conditions screened in this state: 35
  • 3-methylcrotonyl-CoA carboxylase deficiency
  • 3-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

Contacts and Support

State Newborn Screening Program

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

Additional Resources

For a listing of general support, advocacy, and informational resources for Newborn Screening, visit the Resources page.

Date Last Reviewed:
March 2025
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