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  3. West Virginia

West Virginia

State Newborn Screening Panel

Total number of conditions screened in this state: 34
  • 3 methylcrotonyl-CoA carboxylase deficiency
  • Adrenoleukodystrophy
  • Argininosuccinic acidemia
  • Beta-ketothiolase deficiency
  • Biotinidase deficiency
  • Carnitine uptake deficiency
  • Citrullinemia
  • Congenital adrenal hyperplasia
  • Congenital hypothyroidism
  • Critical congenital heart disease
  • Cystic fibrosis
  • Galactosemia
  • Glutaric acidemia
  • Hb disease (C, D, E)
  • Hearing loss
  • Homocystinuria
  • Hydroxy 3 methylglutaric-CoA lyase
  • Isovaleric acidemia
  • Long-chain 3-OH acyl-CoA dehydrogenase deficiency
  • Maple syrup urine disease
  • Medium-chain acyl-CoA dehydrogenase deficiency
  • Methylmalonic acidemia Cbl A and Cbl B forms
  • Methylmalonic acidemia due to mutase deficiency
  • Multiple carboxylase deficiency
  • Phenylketonuria
  • Propionic acidemia
  • S,C disease
  • Severe combined immunodeficiency disease
  • Sickle cell anemia
  • Spinal muscular atrophy
  • Thalassemia
  • Trifunctional protein deficiency
  • Tyrosinemia type 1
  • Very long chain acyl-CoA dehydrogenase deficiency

Contacts and Support

State Newborn Screening Program

West Virginia Newborn Screening

Phone: 304-558-4448
Phone (alt.): 304-414-0797
FAX: 304-957-7549
Email: Deborah.S.Templin@wv.gov
West Virginia Newborn Screening Website

Additional Resources

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

Date Last Reviewed:
December 2022
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