Newborn Screening in Delaware

Delaware Newborn Screening Program
Phone: 302-608-5735
FAX: 302-661-7227

Delaware Newborn Screening Program Website

 

Total number of conditions screened in this state: 47

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
Congenital hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Galactosemia
Glutaric acidemia type II, Multiple acyl-CoA dehydrogenase deficiency
Glutaric acidemia, type I
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
Mitochondrial acetoacetyl-CoA thiolase deficiency
Mucopolysaccharidosis type I
Multiple carboxylase deficiency
Newborn hearing screening
Phenylketonuria
Pompe disease
Proprionic 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

 

Last Reviewed 03/01/2023