Pennsylvania Newborn Screening Program

The Pennsylvania Newborn Screening Program tests all newborns for certain genetic, metabolic, and health disorders shortly after birth. A small blood sample is collected via a heel prick and analyzed to identify conditions like hearing loss and metabolic diseases that may not be obvious at birth but can cause serious health issues if not treated early. Early detection allows for prompt intervention, helping affected infants lead healthier lives. This program is vital for ensuring that babies receive timely care, improving long-term health outcomes and preventing lifelong disabilities.