Bill
Bill > HB1715
summary
Introduced
07/10/2025
07/10/2025
In Committee
07/10/2025
07/10/2025
Crossed Over
Passed
Dead
Introduced Session
2025-2026 Regular Session
Bill Summary
Amending the act of September 9, 1965 (P.L.497, No.251), entitled "An act requiring physicians, hospitals and other institutions to administer or cause to be administered tests for genetic diseases upon infants in certain cases," further providing for Newborn Child Screening and Follow-up Program.
AI Summary
This bill amends the Newborn Child Testing Act to add Duchenne muscular dystrophy (DMD) to the list of diseases that are part of the state's mandatory newborn screening program. Duchenne muscular dystrophy is a severe genetic disorder that causes progressive muscle weakness and typically affects male children, leading to significant disability and shortened life expectancy. By adding this condition to the screening program, the bill aims to help healthcare providers identify infants with DMD early, which can enable timely medical interventions, potential treatments, and support services that could help manage the condition and potentially improve outcomes for affected children. The amendment requires the Pennsylvania Department of Health, with approval from the Newborn Screening and Follow-up Technical Advisory Board, to include Duchenne muscular dystrophy testing as part of the standard newborn screening tests. The bill will take effect 60 days after its enactment, giving healthcare providers and laboratories time to implement the new screening protocol.
Committee Categories
Health and Social Services
Sponsors (5)
Last Action
Laid on the table (on 11/18/2025)
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