181 Neb. Admin. Code, ch. 2, § 003

Current through September 17, 2024

Section 181-2-003 - SPECIFICATION OF DISEASES

All infants born in the state of Nebraska must be tested for the diseases identified in Neb. Rev. Stat. § 71-519 and the following diseases:

(A) Argininosuccinic Acidemia;

(B) Beta-ketothiolase Deficiency;

(C) Carnitine Uptake Defect;

(D) Citrullinemia;

(E) Congenital Adrenal Hyperplasia;

(F) Cystic Fibrosis;

(G) Glutaric Acidemia type 1;

(H) Homocystinuria;

(I) Isovaleric Acidemia;

(J) Long-chain Hydroxyacyl-CoA Dehydrogenase Deficiency;

(K) Maple Syrup Urine Disease;

(L) Methylmalonic Acidemia (Mutase Deficiency);

(M) Methylmalonic Acidemia (Cbl A and B);

(N) Multiple Carboxylase Deficiency;

(O) Propionic Acidemia;

(P) Severe Combined Immune Deficiencies;

(Q) Tyrosinemia;

(R) Trifunctional Protein Deficiency;

(S) Very Long-chain Acyl-CoA Dehydrogenase Deficiency;

(T) 3-Hydroxy 3-Methyl Glutaric Aciduria; and

(U) 3-Methylcrotonyl-CoA Carboxylase Deficiency.

181 Neb. Admin. Code, ch. 2, § 003

Adopted effective 6/5/2018

Amended effective 9/21/2020

Amended effective 9/17/2024