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Georgia

State Newborn Screening Panel

Total number of conditions screened in this state: 37
  • 3 methylcrotonyl-Co A carboxylase deficiency
  • 3-OH 3-CH glutaric aciduria
  • Argininosuccinic acidemia
  • Beta ketothiolase
  • Biotinidase deficiency
  • Carnitine uptake defect
  • Citrullinemia
  • Cobalamin A and B deficiency
  • Congenital adrenal hyperplasia
  • Congenital hypothyroidism
  • Critical congenital heart disease
  • Cystic fibrosis
  • Galactosemia
  • Glutaric acidemia type I
  • Hearing impairment
  • Homocystinuria
  • Isovaleric acidemia
  • Krabbe disease
  • Long chain 3 hydroxyl acyl-CoA dehydrogenase deficiency
  • Maple syrup urine disease
  • Medium chain acyl-CoA dehydrogenase deficiency
  • Methylmalonic acidemia
  • Mucopolysaccharidosis I
  • Multiple carboxylase deficiency
  • Other hemoglobin variants
  • Phenylketonuria
  • Pompe disease
  • Propionic acidemia
  • Severe combined immunodeficiency
  • Sickle beta thalassemia
  • Sickle C disease
  • Sickle cell anemia
  • Spinal muscular atrophy
  • Trifunctional protein deficiency
  • Tyrosinemia
  • Very long-chain acyl-CoA dehydrogenase deficiency
  • X-linked adrenoleukodystrophy

Contacts and Support

State Newborn Screening Program

Georgia Newborn Screening Program

Phone: 404-657-4143
Phone (alt.): 404-327-7900
Georgia 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:
December 2022
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