Genetic Testing for Pediatric Disorders

Genetic testing for pediatric disorders involves analyzing a child's DNA to identify changes or mutations that may cause or increase the risk of specific health conditions. This testing can help diagnose unexplained symptoms, guide treatment options, and inform families about possible hereditary conditions. It can be particularly valuable for conditions that develop in childhood, such as certain genetic syndromes or inherited diseases. Parents can discuss the need for such testing with healthcare providers to understand the potential benefits, risks, and implications for their child's health and family planning.