Delaware | Newborn Screening

State Newborn Screening Panel

2-methylbutyryl-CoA dehydrogenase deficiency
3-hydroxy-3-methylglutaryl-CoA lyase deficiency
3-methylcrotonyl-CoA carboxylase deficiency
Argininemia
Argininosuccinate lyase deficiency
Argininosuccinate synthetase deficiency (Citrullinemia)
Biotinidase deficiency
Carnitine palmitoyltransferase II deficiency
Carnitine uptake deficiency
Carnitine/acylcarnitine translocase deficiency
Congenital adrenal hyperplasia
Critical congenital heart disease
Cystic fibrosis
Galactosemia
Glutaric acidemia type II, Multiple acyl-CoA dehydrogenase deficiency
Glutaric acidemia, type I
Glycogen storage disease type II
Holocarboxylase Synthase Deficiency (Multiple Carboxylase Deficiency- MCD)
Homocystinuria
Hypermethioninemia
Hyperphenylalaninemia
Isobutyryl-CoA dehydrogenase deficiency
Isovaleric acidemia
Long-chain hydroxyacyl-CoA dehydrogenase deficiency
Maple syrup urine disease
Medium chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia (cobalamin disorders)
Methylmalonic acidemia (methylmalonyl-CoA mutase)
Methylmalonic acidemia with homocystinuria (Cbl C,D)
Mitochondrial acetoacetyl-CoA thiolase deficiency
Mucopolysaccharidosis type I
Mucopolysaccharidosis type II
Newborn hearing screening
Phenylketonuria
Primary congenital hypothyroidism
Propionic acidemia
SC disease
Severe combined immunodeficiency
Short-chain acyl-CoA dehydrogenase deficiency
Spinal muscular atrophy
SS disease
Trifunctional protein deficiency
Tyrosinemia, type I
Tyrosinemia, type II
Tyrosinemia, type III
Variant Hgb
Very long-chain acyl-CoA dehydrogenase deficiency
X-linked adrenoleukodystrophy

Contacts and Support

State Newborn Screening Program

Delaware Newborn Screening Program

Phone: 302-651-5079

FAX: 302-295-0719

Delaware 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:

June 2026