Ohio Administrative Code
Title 3701 - Department of Health - Administration and Director
Chapter 3701-55 - Newborn Screening for Genetic, Endocrine, or Metabolic Disorders
Section 3701-55-02 - Required screening; facility requirements
Universal Citation: OH Admin Code 3701-55-02
Current through all regulations passed and filed through September 16, 2024
(A) All newborn children shall be screened in accordance with procedures set forth in this chapter for the presence of the following genetic, endocrine, or metabolic disorders:
(1) 2-methylbutyryl-CoA
dehydrogenase deficiency;
(2) 3-hydroxy-3-methylglutaryl-CoA lyase
deficiency;
(3) 3-ketothiolase
deficiency;
(4)
3-methylcrotonyl-CoA carboxylase
deficiency;
(5) Argininemia;
(6) Argininosuccinic acidemia;
(7) Biotinidase deficiency;
(8) Carnitine/acylcarnitine translocase
deficiency;
(9) Carnitine palmitoyl
transferase deficiency type II;
(10) Carnitine uptake defect;
(11) Citrullinemia;
(12) Congenital adrenal
hyperplasia;
(13) Congenital
hypothyroidism;
(14) Cystic
fibrosis;
(15)
Galactosemia;
(16) Glutaric
acidemia type I;
(17) Glutaric
acidemia type II;
(18) Glycogen
storage disease type II (Pompe);
(19) Homocystinuria
(cystathionine-beta-synthase deficiency);
(20) Hypermethioninemia;
(21) Isovaleric
acidemia;
(22) Krabbe
disease;
(23) Long chain
hydroxyacyl-CoA dehydrogenase deficiency;
(24)
Maple syrup urine disease;
(25) Medium
chainacyl-CoA dehydrogenase deficiency;
(26) Methylmalonic
acidemia;
(27)
Mucopolysaccharidosis type 1;
(28) Multiple CoA
carboxylase deficiency;
(29) Phenylketonuria;
(30) Propionic
acidemia;
(31) Severe combined
immune deficiency;
(32) Sickle cell and
other hemoglobinopathies;
(33)
Spinal muscular atrophy (SMA);
(34) Trifunctional protein
deficiency;
(35) Tyrosinemia
type-I;
(36) Tyrosinemia
type-II;
(37) Tyrosinemia type-III;
and
(38) Very long chain acyl-CoA
dehydrogenase deficiency.; and
(39)
X-linked
adrenoleukodystrophy (X-ALD).
(B) All hospitals and freestanding birthing centers that are required by this chapter to cause specimens to be collected for newborn screening for genetic, endocrine, or metabolic disorders shall:
(1) Designate a newborn screening coordinator
and physician responsible for the coordination of the facility's newborn
screening;
(2) Notify the chief of
the Ohio department of health bureau of public laboratories of the name of the
individual designated as the newborn screening coordinator on a yearly basis
and whenever the designated individual changes; and
(3) Develop a written protocol for tracking
newborn screening activities. The protocol must
include a process for documenting the dates of specimen
collection, shipping, and receipt of screening results. The protocol must also
include a requirement that key fields including
date and time of infant birth, date and time of specimen collection, weight of
infant, feeding status, transfusion history, and the name of the
physician attending the child after birth or a designee be placed on the
specimen
demographic form sent with the
specimen to the Ohio department of
health public health laboratory.
Disclaimer: These regulations may not be the most recent version. Ohio may have more current or accurate information. We make no warranties or guarantees about the accuracy, completeness, or adequacy of the information contained on this site or the information linked to on the state site. Please check official sources.
This site is protected by reCAPTCHA and the Google
Privacy Policy and
Terms of Service apply.