Wisconsin

Wisconsin Newborn Screening
Phone: 608-890-1796
Email: Mei.Baker@wisc.edu

Wisconsin Newborn Screening Website

 

Total number of conditions screened in this state: 49

2,4-Dienoyl-CoA reductase deficiency
2-methyl-3-hydroxybutyryl CoA dehydrogenase deficiency
3-hydroxy-3-methylglutaryl-CoA lyase deficiency
3-methylcrotonyl CoA carboxylase deficiency
3-methylglutaconyl CoA hydratase deficiency
Argininosuccinic acidemia
Biotinidase deficiency
Carnitine palmitoyl transferase deficiency type IA
Carnitine palmitoyl transferase deficiency type II
Carnitine uptake defect
Carnitine/acylcarnitine translocase deficiency
Citrullinemia type I
Citrullinemia type II
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Galactosemia
Glutaryl CoA dehydrogenase deficiency type I aka Glutaric acidemia type I
Glutaryl CoA dehydrogenase deficiency type II aka Glutaric acidemia type II
Hearing loss
Hemoglobin S-beta thalassemia
Hemoglobin S/C disease
Homocystinuria
Hypermethioninemia
Hyperphenylalaninemia
Isovaleryl CoA dehydrogenase deficiency aka Isovaleric acidemia
Long chain 3-hydroxyacyl CoA dehydrogenase deficiency
Maple syrup urine disease
Medium chain 3-ketoacyl-CoA thiolase deficiency
Medium chain acyl-CoA dehydrogenase deficiency
Medium/short chain hydroxylacyl CoA dehydrogenase
Methylmalonic acidemia Cbl A & B
Methylmalonic acidemia mutase
Methylmalonic acidemia: Cbl C & D
Mitochondrial acetoacetyl CoA thiolase deficiency
Multiple CoA carboxylase deficiency
Phenylketonuria
Pompe disease
Propionyl CoA carboxylase deficiency aka Propionic acidemia
Severe combined immune deficiency
Sickle cell disease
Spinal muscular atrophy
Trait and Variant Hemoglobins
Trifunctional protein deficiency
Tyrosinemia type I
Tyrosinemia type II
Tyrosinemia type III
Very long chain acyl-CoA dehydrogenase deficiency

 

Last Reviewed 03/01/2023