Neonatal Screening for Genetic Disorders

Neonatal screening for genetic disorders is a simple blood test performed on newborns shortly after birth. It identifies certain genetic, endocrine, and metabolic disorders that may not be immediately apparent but can cause serious health issues if untreated. The goal is to detect these conditions early, allowing for prompt treatment and better health outcomes. Common disorders screened include phenylketonuria (PKU) and cystic fibrosis. Parents usually receive the results within a few weeks, and if a disorder is detected, further testing and medical guidance follow to ensure the child receives appropriate care.