Newborn Metabolic Screening

Newborn metabolic screening is a testing process performed shortly after birth to detect certain rare but serious conditions related to how the body processes nutrients. A small blood sample is taken from the baby’s heel and analyzed for signs of metabolic disorders that, if identified early, can often be treated effectively. The goal is to catch conditions like certain genetic disorders before symptoms appear, preventing complications such as developmental delays or health problems. This screening is a vital step in ensuring the baby's long-term health and well-being.