Kansas Newborn Screening Program
Phone: 785-291-3363
FAX: 785-559-4245
Email: kdhe.newbornscreening@ks.gov
Kansas Newborn Screening Program Website
Total number of conditions screened in this state: 38
3-hydroxy-3methylglutaryl-CoA lyase deficiency3-methylcrotonyl-CoA carboxylase deficiency
Argininosuccinic acidemia
Beta ketothiolase
Biotinidase deficiency
Carnitine uptake defect
Citrullinemia
Congenital adrenal hyperplasia
Critical congenital heart disease
Cystic fibrosis
Galactosemia
Glutaric acidemia type I
Hearing loss
Hemoglobin SC disease
Holocarboxylase synthetase deficiency
Homocystinuria
Isovaleric acidemia
Long chain hydroxy acyl-CoA dehydrogenase deficiency
Long-chain L-3 hydroxyacyl-CoA dehydrogenase
Maple syrup urine disease
Medium chain acyl-CoA dehydrogenase deficiency
Methylmalonic Acidemia—Cobalamin disorders
Methylmalonyl-CoA mutase deficiency
MPS I (Hurler syndrome)
Phenylketonuria
Pompe
Primary congenital hypothyroidism
Propionic acidemia
Severe combined immunodeficiency
Sickle beta-thalassemia
Sickle C disease
Sickle cell anemia
Sickle cell disease
Spinal muscular atrophy
Trifunctional protein deficiency
Tyrosinemia type I
Very long chain acyl-CoA dehydrogenase deficiency
βeta-ketothiolase deficiency
Last Reviewed 03/01/2023