South Dakota Statutes
§ 34-24-18 — Phenylketonuria, hypothyroidism, and galactosemia testing in newborn.
South Dakota § 34-24-18
This text of South Dakota § 34-24-18 (Phenylketonuria, hypothyroidism, and galactosemia testing in newborn.) is published on Counsel Stack Legal Research, covering South Dakota primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.
Bluebook
S.D. Codified Laws § 34-24-18 (2026).
Text
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.
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Legislative History
SL 1973, ch 233, § 8; SL 1982, ch 264, § 2; SL 1991, ch 277, § 1; SL 2015, ch 185, § 2.
Nearby Sections
15
§ 34-1-1
§ 34-1-1§ 34-1-1.1
Department reorganized and continued.§ 34-1-15
§ 34-1-15§ 34-1-19
Repealed§ 34-1-2
, 34-1-2.1Cite This Page — Counsel Stack
Bluebook (online)
South Dakota § 34-24-18, Counsel Stack Legal Research, https://law.counselstack.com/statute/sd/34-24-18.