Newborn Screening Program

The Newborn Screening Program is a public health initiative that tests newborns shortly after birth for certain serious but treatable conditions. Using a small blood sample, healthcare professionals look for genetic disorders, hormonal issues, and metabolic problems that could affect the baby’s health. Early detection is crucial, as it allows for timely interventions that can prevent severe health complications, developmental delays, or even death. Parents are usually informed about the screening process and results, ensuring that any necessary follow-up can be promptly addressed, supporting the child’s long-term health and development.