infant screening

Infant screening involves testing newborns shortly after birth to detect certain health conditions, genetic disorders, or diseases that may not be immediately apparent. Early identification allows for timely treatment, which can prevent serious health problems, developmental delays, or complications. These screenings typically include a small blood sample, hearing tests, and other assessments, depending on the country’s protocols. The goal is to ensure that any potential issues are caught early, so appropriate interventions can be provided to support the infant’s health and development.