The tests for detecting a metabolic, inherited, or genetic disorder of the newborn infant, as prescribed by the Department of Health, shall include the testing for excessive phenylalanine in the serum of the newborn, for hypothyroidism, and for elevated blood galactose in the newborn.
S.D. Codified Laws § 34-24-18
Phenylketonuria, hypothyroidism, and galactosemia testing in newborn
Source: SL 1973, ch 233, § 8; SL 1982, ch 264, § 2; SL 1991, ch 277, § 1; SL 2015, ch 185, § 2.
Official source: South Dakota Legislature. Reproduced from public-domain South Dakota statutes; confirm against the official source for the current text. Not legal advice.