What was one objective of the Newborn Screening Act?

One primary objective of the Newborn Screening Act is to screen newborns for certain genetic conditions. This legislation was established to ensure that all newborns are tested for a variety of genetic, metabolic, hormonal, and functional conditions that, if left untreated, could lead to severe health issues or disabilities. Early detection can result in timely intervention, which significantly improves health outcomes and quality of life for affected infants.

The legislation emphasizes the importance of identifying such conditions at an early stage, allowing for proactive measures, including treatment, management, and family support, thereby reducing morbidity associated with undiagnosed conditions. By implementing these screening programs, the Act aims to promote the health and well-being of newborns and provide parents with essential health information.

Other options do not accurately reflect the primary aim of the Newborn Screening Act. While eliminating congenital disorders is a broader goal of public health, it is not a specific objective of this legislation. Providing free health care to all children extends beyond the scope of newborn screening and targets healthcare access rather than screening. The education of health workers is important for the healthcare system but is not the central focus of the Act. The key emphasis remains on the identification and management of specific conditions through early screening.