Current through Register Vol. 35, No. 20, October 22, 2024
Section 7.30.6.8 - DISORDERSA. 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;(8) congenital adrenal hyperplasia;(9) congenital hypothyroidism;(12) glutaric academia type I;(13) Hb S/beta-thalassemia;(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;(25) trifunctional protein deficiency;(26) tyrosinemia type I; and(27) very long-chain acyl-CoA dehydrogenase deficiency.N.M. Admin. Code § 7.30.6.8
7.30.6.8 NMAC - N, 10/30/12