Phenylketonuria, hypothyroidism, and galactosemia testing in newborn

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. Source: SL 1973, ch 233 , § 8; SL 1982, ch 264 , § 2; SL 1991, ch 277 , § 1; SL 2015, ch 185 , § 2.