New Mexico | Newborn Screening

State Newborn Screening Panel

2-methyl-3-hydroxybutyryl CoA dehydrogenase deficiency
2-methylbutyryl CoA dehydrogenase deficiency
3-hydroxy-3-methylglutaryl CoA lyase deficiency
3-methylcrotonyl CoA carboxylase deficiency
3-methylglutaconyl CoA hydratase deficiency
Arginase deficiency
Argininosuccinate lyase deficiency
Beta-ketothiolase deficiency
Biotinidase deficiency
Carnitine acylcarnitine translocase deficiency
Carnitine palmitoyl transferase deficiency, type I
Carnitine palmitoyl transferase deficiency, type II
Carnitine uptake defect
Citrullinemia, type I
Congenital adrenal hyperplasia
Critical congenital heart disease
Cystic fibrosis
Fabry
Galactosemia
Gaucher
Glutaric acidemia type II
Glutaric acidemia, type I
Hearing deficiency
Hemoglobinopathies
Homocystinuria
Hypermethioninemia
Isobutyryl-CoA dehydrogenase deficiency
Isovaleric acidemia
Long chain 3 hydroxyacyl-CoA dehydrogenase deficiency
Malonic acidemia
Maple syrup urine disease
Medium chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia (cobalamin disorders)
Methylmalonic acidemia (methylmalonyl-CoA mutase deficiency)
Methylmalonic acidemia with homocystinuria
Mucopolysaccharidosis type I
Multiple carboxylase deficiency
Phenylketonuria
Pompe
Primary congenital hypothyroidism
Propionic acidemia
S, Beta-thalassemia
S,C disease
Severe combined immunodeficiency
Short chain acyl-CoA dehydrogenase deficiency
Sickle cell anemia
Spinal muscular atrophy
Trifunctional protein deficiency
Tyrosinemia, type I
Tyrosinemia, type II
Tyrosinemia, type III
Very long chain acyl-CoA dehydrogenase deficiency
X-linked adrenoleukodystrophy

In this state, babies undergo a second screening step when they are around two weeks old. This second screening usually happens in a health care provider’s office. It can help find babies who have conditions that are hard to detect in the first days of life but that still benefit from early treatment or intervention.

Contacts and Support

State Newborn Screening Program

New Mexico Newborn Genetic Screening Program

Phone: 505-476-8858

Phone (alt.): 877-890-4692

Email: carlaa.ortiz@doh.nm.gov

New Mexico Newborn Genetic Screening Program Website

Early Hearing Detection and Intervention

New Mexico EHDI Program

Phone: 877-890-4692

New Mexico EHDI Program Website

Additional Resources

For a listing of general support, advocacy, and informational resources for Newborn Screening, visit the Resources page.

Date Last Reviewed:

September 2024