Bill
Bill > SB269
summary
Introduced
02/20/2025
02/20/2025
In Committee
02/20/2025
02/20/2025
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 expand the state's Newborn Child Screening and Follow-up Program by adding Duchenne muscular dystrophy (DMD) to the list of diseases for which newborns are screened. Duchenne muscular dystrophy is a rare, progressive genetic disorder characterized by muscle weakness and degeneration that primarily affects male children. The bill requires the state department of health, with approval from the Newborn Screening and Follow-up Technical Advisory Board, to include DMD screening tests as part of its existing newborn screening program. The purpose of this screening is to help healthcare providers identify potential cases early, which could allow for earlier intervention, treatment, or services to mitigate the potential intellectual or physical disabilities associated with the condition. The bill will take effect 60 days after its enactment, ensuring that the new screening protocol can be implemented in a timely manner.
Committee Categories
Health and Social Services
Sponsors (12)
Amanda Cappelletti (D)*,
Lisa Baker (R),
Maria Collett (D),
Carolyn Comitta (D),
Jay Costa (D),
Art Haywood (D),
John Kane (D),
Nick Miller (D),
Steve Santarsiero (D),
Nikil Saval (D),
Judy Schwank (D),
Tina Tartaglione (D),
Last Action
Referred to Health & Human Services (on 02/20/2025)
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