Pediatric Genomic Medicine

Pediatric genomic medicine is a branch of healthcare that uses genetic information to understand and treat health issues in children. By analyzing a child’s DNA, doctors can identify genetic disorders, predict risks for certain diseases, and tailor treatments to each child’s unique genetic makeup. This approach not only helps in diagnosing conditions earlier but also allows for more effective and personalized therapies. As research advances, it aims to improve outcomes for children with rare or complex health problems by harnessing the power of genetics in clinical practice.