New Mexico Administrative Code
Title 7 - HEALTH
Chapter 30 - FAMILY AND CHILDREN HEALTH CARE SERVICES
Part 6 - NEWBORN GENETIC SCREENING PROGRAM
Section 7.30.6.8 - DISORDERS
Universal Citation: 7 NM Admin Code 7.30.6.8
Current through Register Vol. 35, No. 18, September 24, 2024
A. Disorders for which screening shall be performed include the following:
(1) 3-mthylcrotonyl-CoA deficiency;
(2) 3-OH 3-CH3 glutaric aciduria;
(3) argininosuccinic academia;
(4) mitochondrial acetoacetyl-CoA;
(5) biotinidase deficiency;
(6) carnitine uptake defect;
(7) citrullinemia;
(8) congenital adrenal hyperplasia;
(9) congenital hypothyroidism;
(10) cystic fibrosis;
(11) galactosemia;
(12) glutaric academia type I;
(13) Hb S/beta-thalassemia;
(14) hearing deficiency;
(15) homocystinuria;
(16) isovaleric academia;
(17) long-chain L-3-OH acyl-CoA dehydrogenase
deficiency;
(18) maple syrup urine
disease;
(19) medium chain acyl-CoA
dehydrogenase deficiency;
(20)
methylmalonic academia;
(21)
multiple carboxylase deficiency;
(22) phenylketonuria;
(23) proponic academia;
(24) sickle cell anemia;
(25) trifunctional protein
deficiency;
(26) tyrosinemia type
I; and
(27) very long-chain
acyl-CoA dehydrogenase deficiency.
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