Newborn Screening

Newborn screening is a crucial public health initiative that tests infants for genetic, endocrine, and metabolic disorders shortly after birth. Early detection allows for timely interventions, significantly improving health outcomes. This proactive approach ensures that infants receive necessary care before symptoms appear.

Our newborn screening services employ advanced technologies to identify conditions that can impact a child’s health. By providing early diagnosis, we help families access appropriate treatments and support for their children’s well-being.