neonatal screening programs

Neonatal screening programs are tests conducted on newborns shortly after birth to identify potential genetic, metabolic, or other health conditions. These screenings help detect disorders that may not be immediately visible but can lead to serious health issues if untreated. By identifying these conditions early, healthcare providers can initiate timely interventions and treatments, significantly improving the child’s long-term health outcomes. Commonly screened conditions include phenylketonuria (PKU) and congenital hypothyroidism. The aim is to ensure all newborns receive a healthy start in life by catching potential problems early on.