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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