100 chapters · 1,735 sections in this title.
SDCL § 34-24-16 Educational program on metabolic diseases
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The State Department of Health shall provide for the development and carrying out of an educational program among physicians, staffs of hospitals, public health nurses, and the citizens of this state concerning the disease phenylketonuria, hypothyroidism, and other metabolic dise…
SDCL § 34-24-17 Screening of newborn infants for metabolic, inherited, and genetic disorders
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Each infant born in South Dakota shall be screened for metabolic, inherited, and genetic disorders. This screening shall be as prescribed by the Department of Health. Source: SL 1973, ch 233 , § 2; SL 1990, ch 170 , § 8; SL 2015, ch 185 , § 1.
SDCL § 34-24-18 Phenylketonuria, hypothyroidism, and galactosemia testing in newborn
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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 new…
SDCL § 34-24-19 Phenylketonuria, hypothyroidism, or galactosemia tests when facilities not available
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If facilities are not available for the screening of newborn infants for the phenylketonuria syndrome, for hypothyroidism or for galactosemia, the Department of Health shall arrange for testing through the director of laboratories. Source: SL 1973, ch 233 , § 7; SL 1982, ch 264 ,…