Question
What is a newborn genetic metabolic disorder test? Why is it so important for families with a history of adverse pregnancy?
Answer
A newborn genetic metabolic disorder test is a method to screen for congenital genetic diseases in newborns through a simple blood spot test. This method is fast, inexpensive, and can detect genetic metabolic disorders early, allowing for timely treatment to ensure the child’s healthy growth. For families with a history of adverse pregnancy, this test is particularly important as it helps to identify potential genetic issues early on and take appropriate intervention measures to reduce the harm of genetic metabolic disorders to the child’s health.