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Arkansas

State Newborn Screening Panel

Total number of conditions screened in this state: 31
  • 3-hydroxy-3-methyl glutaric acidemia
  • 3-methylcrotonyl CoA carboxylase deficiency
  • 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, type I
  • Hearing loss
  • Homocystinuria
  • Isovaleric acidemia
  • Long chain hydroxyacyl CoA dehydrogenase deficiency
  • Maple syrup urine disease
  • Medium chain acyl CoA dehydrogenase deficiency
  • Methylmalonic acidemia due to cobalamin A,B defect
  • Methylmalonic acidemia due to mutase deficiency
  • Multiple carboxylase deficiency
  • Phenylketonuria
  • Propionic acidemia
  • Severe combined immunodeficiency
  • Sickle - hemoglobin C disease
  • Sickle cell disease
  • Sickle-beta-thalassemia
  • Trifunctional protein deficiency
  • Tyrosinemia, type 1
  • Very long chain acyl CoA dehydrogenase deficiency

Contacts and Support

State Newborn Screening Program

Arkansas Newborn Screening Program

Phone: 866-769-9043
FAX: 501-280-4769
Arkansas Newborn Screening Program Website

Early Hearing Detection and Intervention

Arkansas EHDI Program

Phone: 501-280-4740
Email: adhinfanthearing@arkansas.gov
Arkansas EHDI 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 2022
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