Description

Newborn Screening is a program that identifies babies at risk of having rare, but serious medical conditions that can affect normal development. These Newborn Screening may combines as many as 48 biochemical testing of metabolic & genetic conditions with confirmatory genetic testing for screen-positive results

Pre-Information

Clinical history, suspicion of metabolic diseases or inborn errors of metabolism, fasting recommendation but not requirement, and preliminary diagnosis of the clinician are all necessary.