Hawaii Newborn Metabolic Screening Program
Phone: 808-733-9069
FAX: 808-733-9071
Email: dana.mulcahy@doh.hawaii.gov
Hawaii Newborn Metabolic Screening Program Website
Total number of conditions screened in this state: 35
3-hydroxy-3-methylglutaric aciduriaAlpha thalassemia (Barts)
Argininosuccinic acidemia
Beta-ketothiolase deficiency
Biotinidase deficiency
Carnitine uptake deficiency
Citrullinemia
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart defects
Critical congenital heart disease
Cystic fibrosis
Galactosemia
Glutaric acidemia type I
Hearing loss
Hemoglobin C trait
Hemoglobin D trait
Hemoglobin E trait
Hemoglobin S trait
Hemoglobinopathies
Homocystinuria
Isovaleric acidemia
Long-chain L-3-hydroxy acyl-CoA dehydrogenase deficiency
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia (Cbl A,B)
Methylmalonic acidemia (mutase deficiency)
Multiple carboxylase deficiency
Phenylketonuria
Propionic acidemia
Severe combined immunodeficiency
Sickle cell diseases
Trifunctional protein deficiency
Tyrosinemia type 1
Very-long chain acyl-CoA dehydrogenase deficiency
Last Reviewed 03/01/2023