Administrative Rules of Montana
Department 37 - PUBLIC HEALTH AND HUMAN SERVICES
Chapter 37.57 - MATERNAL AND CHILD HEALTH
Subchapter 37.57.3 - Infant Screening Tests and Eye Treatment
Rule 37.57.301 - DEFINITIONS
Universal Citation: MT Admin Rules 37.57.301
Current through Register Vol. 18, September 20, 2024
As used in this subchapter, the following definitions apply:
(1) "Health care facility" means a hospital or other facility licensed by or located in the state of Montana for the purpose of providing health care services, and which provides primary health care services for newborns at birth.
(2) "Newborn" means an infant in the first 28 days of life.
(3) "Newborn screening tests" are screening tests, procedures, or both for the following conditions:
(a) Acylcarnitine Disorders:
(i) Fatty Acid Oxidation Disorders:
(A) Carnitine uptake defect;
(B) Long-chain L-3-OH acyl-CoA dehydrogenase
deficiency;
(C) Medium-chain
acyl-CoA dehydrogenase deficiency;
(D) Trifunctional protein deficiency;
and
(E) Very long-chain acyl-CoA
dehydrogenase deficiency;
(ii) Organic Acidemia Disorders:
(A) 3-hydroxy-3-methylglutaryl-CoA lyase
deficiency;
(B)
3-Methylcrotonyl-CoA carboxylase deficiency;
(C) [BETA]-ketothiolase deficiency;
(D) Glutaric acidemia type I;
(E) Isovaleric acidemia;
(F) Methylmalonic acidemia (Cbl
A,B);
(G) Methylmalonic acidemia
(mutase deficiency);
(H) Multiple
carboxylase deficiency; and
(I)
Propionic acidemia;
(b) Amino Acid Disorders:
(i) Argininosuccinic acidemia;
(ii) Citrullinemia type 1;
(iii) Homocystinuria;
(iv) Maple syrup urine disease;
(v) Classic Phenylketonuria; and
(vi) Tyrosinemia type I;
(c) Biotinidase deficiency;
(d) Classical galactosemia;
(e) Congenital adrenal hyperplasia;
(f) Primary congenital
hypothyroidism;
(g) Cystic
fibrosis;
(h) Hemoglobinopathies,
including:
(i) Hb S/[BETA]
-thalassemia;
(ii) Hb SC disease;
and
(iii) Hb SS disease;
and
(i) Critical
congenital heart disease, including:
(i)
hypoplastic left heart syndrome;
(ii) pulmonary atresia;
(iii) tetralogy of Fallot;
(iv) total anomalous pulmonary venous
return;
(v) transposition of the
great arteries;
(vi) tricuspid
atresia;
(vii) truncus
arteriosus;
(j) Severe
combined immunodeficiency disease;
(k) Spinal muscular atrophy (SMA);
and.
(l) X-linked
adrenoleukodystrophy (X-ALD).
AUTH: 50-19-202, MCA; IMP: 50-19-203, MCA
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