Ga. Comp. R. & Regs. R. 511-5-5-.03 - Testing Required of Newborn Babies
(1)
It is the goal of the Department that every baby born alive in Georgia shall be
tested for the following conditions, unless its parents or legal guardians
object in writing on the ground that such tests and treatment conflict with
their religious beliefs:
(a) critical
congenital heart disease (CCHD);
(b) hearing impairment;
(c) argininosuccinic aciduria;
(d) beta-ketothiolase deficiency;
(e) biotinidase deficiency;
(f) carnitine uptake defect;
(g) citrullinemia;
(h) congenital adrenal hyperplasia;
(i) congenital hypothyroidism;
(j) cystic fibrosis;
(k) galactosemia;
(l) glutaric acidemia type I;
(m) homocystinuria;
(n) isovaleric acidemia;
(o) Krabbe disease as a pilot program
beginning September 21, 2021;
(p)
long-chain acyl-CoA dehydrogenase deficiency;
(q) maple syrup urine disease;
(r) medium-chain acyl-CoA dehydrogenase
deficiency;
(s) methylmalonic
acidemia;
(t) mucopolysaccharidosis
type 1;
(u) multiple carboxylase
deficiency;
(v)
phenylketonuria;
(w) pompe
disease;
(x) propionic
acidemia;
(y) severe combined
immunodeficiency (SCID);
(z) sickle
cell hemoglobinopathies;
(aa) spinal
muscular atrophy;
(bb)
trifunctional protein deficiency;
(cc) tyrosinemia;
(dd) very long-chain acyl-CoA dehydrogenase
deficiency;
(ee) x-linked
adrenoleukodystrophy;
(ff)
3-methylcrotonyl-CoA carboxylase deficiency; and
(gg) 3-OH 3-CH3 glutaric
aciduria.
(2) Unless
otherwise noted in subparagraph (1) above, testing for conditions (1)(c)
through (gg) shall be conducted through laboratory analysis of the baby's blood
on a Newborn Screening Specimen Card as provided in DPH Rule
511-5-5-.04.
Notes
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