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2000 SESSION
003646836Be it enacted by the General Assembly of Virginia:
1. That § 32.1-67 of the Code of Virginia is amended and reenacted as follows:
§ 32.1-67. Duty of Board with respect to treatment.
The Board shall recommend procedures for the treatment of biotinidase
deficiency, phenylketonuria, hypothyroidism, homocystinuria, galactosemia,
Maple Syrup Urine Disease and sickle cell diseases, and shall provide such
treatment for infants in medically indigent families. The Board shall create
procedures to provide to (i) the parents or guardian of any child or (ii) to
any pregnant woman, who is a legal resident of the Commonwealth and who is
diagnosed as requiring treatment for phenylketonuria, the special food products
required in the management of phenylketonuria out of such funds as may be
appropriated for this purpose. The special food products shall include medical
formulas which are designed specifically for the treatment of phenylketonuria and low
protein modified foods (not foods naturally low in protein) which are designed
specifically for use in the treatment for inborn errors of metabolism. The
parents or guardian of any such child, or the pregnant woman, shall, in the
discretion of the Department, reimburse to the local health department the cost of such
special food products medical formulas in an amount not to exceed two percent
of their gross income. The parents or guardian of any such child, or the
pregnant woman, shall, with such funds as are appropriated, receive reimbursement
from the Department for the cost of such special low protein modified foods in
an amount not to exceed $2,000 per diagnosed person per year. The
reimbursement required by this section shall be payable quarterly by the first day of
January, April, July, and October.