Why is DNA Sequencing Important for Neonatal Disorders?
DNA sequencing is the process of determining the exact order of nucleotides within a DNA molecule. This is vital for diagnosing hereditary diseases and other genetic conditions in newborns. By identifying specific genetic markers, healthcare providers can diagnose conditions early, potentially even before symptoms appear. Early diagnosis allows for timely intervention and better management of the disorder, improving the long-term outcomes for affected infants.
