An Act amending the act of September 9, 1965 (P.L.497, No.251), known as the Newborn Child Testing Act, further providing for Newborn Child Screening and Follow-up Program.

HB 1652 adds Gaucher disease to Pennsylvania's mandatory newborn screening program under the Newborn Child Testing Act. The bill expands the existing program to require screening for this genetic disorder in newborns, directly affecting all infants born in Pennsylvania. Key provisions include updating the list of covered conditions under Section 3(a)(1) of the 1965 Act, ensuring healthcare providers screen for Gaucher disease to identify it early. This change aims to enable timely treatment to prevent intellectual or physical disabilities, aligning with the program's existing purpose. The bill does not alter funding or implementation processes, only adding one specific condition to the screening list.