Ch. 1, § 4. Wyoming Newborn Screening Panel

(a) As determined by the committee established under W.S. 35-4-801(b), the Wyoming Newborn Screening Panel must include the following tests for metabolic and genetic conditions: (i) Initial bloodspot specimen collection performed according to section 5 of this Chapter, which screens for amino acid disorders, endocrine disorders, fatty acid oxidation disorders, hemoglobin disorders, organic acid disorders, and other metabolic and genetic disorders. (ii) Second bloodspot specimen collection performed according to section 6 of this Chapter, which screens for an abbreviated panel; and (iii) Pulse oximetry screening performed according to section 7 of this Chapter, which screens for critical congenital heart disease (CCHD).