Newborn Screening in Louisiana

Louisiana Newborn Screening Program
Phone: 504-568-8254
FAX: 504-568-8253
Email: Cheryl.harris@la.gov

Louisiana Newborn Screening Program Website

 

Total number of conditions screened in this state: 33

3-methylcrotonyl-CoA carboxylase deficiency
3-OH 3-CH3 glutaric aciduria
Argininosuccinic aciduria
Biotinidase deficiency
Carnitine uptake defect
Citrullinemia
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Galactosemia
Glutaric acidemia type I
Glycogen storage diseases type II (Pompe disease)
Hb S/C disease
Hb S/β-thalassemia
Hearing loss
Homocystinuria
Isovaleric acidemia
Long-chain L-3-OH acyl-CoA dehydrogenase deficiency
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia - Cbl A B
Methylmalonic acidemia – mutase deficiency
Mucopolysaccharidosis type I
Multiple carboxylase deficiency
Phenylketonuria
Propionic acidemia
Severe combined immunodeficiency
Sickle cell anemia
Spinal muscular atrophy
Trifunctional protein deficiency
Very long-chain acyl-CoA dehydrogenase deficiency
β-ketothiolase deficiency

 

Last Reviewed 03/01/2023