Phenylketonuria; special foods for management thereof. (HB1607)
Introduced By
Progress
✓ |
Introduced |
✗ |
Passed Committee |
☐ |
Passed House |
☐ |
Passed Senate |
☐ |
Signed by Governor |
☐ |
Became Law |
Description
Special foods for the management of phenylketonuria. Provides for the reimbursement, in an amount not to exceed $ 2,000 per diagnosed person per year, to the parents or guardian of a child identified as being a legal resident of the Commonwealth and who is diagnosed as requiring treatment for phenylketonuria (PKU), for the purchase of special food products required in the management of phenylketonuria. Read the Bill »
Status
02/07/2006: Failed to Pass in Committee
History
Date | Action |
---|---|
01/24/2006 | Unanimous consent to introduce |
01/24/2006 | Presented and ordered printed 062044304 |
01/24/2006 | Referred to Committee on Health, Welfare and Institutions |
01/31/2006 | Fiscal impact statement from DPB (HB1607) |
02/07/2006 | Continued to 2007 in Health, Welfare and Institutions |