West Virginia Statutes

§ 16-22-3 — Tests for diseases specified by the state Public Health Commissioner; reports; assistance to afflicted children; Public Health Commissioner to propose rules

West Virginia·Ch. 16 PUBLIC HEALTH·Art. 22 DETECTION AND CONTROL OF PHENYLKETONURIA, GALACTOSEMIA, HYPOTHYROIDISM, AND CERTAIN OTHER DISEASES IN NEWBORN CHILDREN
(a)The hospital or birthing center in which an infant is born, the parents or legal guardians, the physician attending a newborn child, or any person attending a newborn child not under the care of a physician shall require and ensure that each such child be tested for phenylketonuria, galactosemia, hypothyroidism, sickle cell anemia and certain other diseases specified by the Bureau for Public Health. The Bureau for Public Health shall also require testing for congenital adrenal hyperplasia, cystic fibrosis and biotinidase deficiency. No later than July 1, 2008, the Bureau for Public Health shall also require testing for isovaleric acidemia, glutaric acidemia type I, 3-Hydroxy-3-methylglutaric aciduria, multiple carboxylase deficiency, methylmalonic acidemia-mutase deficiency form, 3-met

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West Virginia § 16-22-3 (Tests for diseases specified by the state Public Health Commissioner; reports; assistance to afflicted children; Public Health Commissioner to propose rules) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

Legislative History

2024 Reg. Sess., HB4978; 2022 Reg. Sess., HB2798; 2016 Reg. Sess., HB4470; 2008 Reg. Sess., HB4513; 2007 Reg. Sess., HB2583; 2006 Reg. Sess., HB2607; 2005 Reg. Sess., HB2607; 2004 Reg. Sess., HB4441; 1991 Reg. Sess., HB2822; 1982 Reg. Sess., SB72; 1978 Reg. Sess., SB369; 1966 Reg. Sess., HB275; 1965 Reg. Sess., SB182

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