TORONTO, Sept. 8, 2016--Newborn screening is considered to be a "baby's first test." Within the first two days of birth, a baby's heel is pricked to obtain a small amount of blood that is screened for up to dozens of genetic diseases, especially those where early detection and treatment can prevent irreversible damage.
However, technological advances have allowed newborn screening to test for hundreds of diseases, including those for which there may be no established treatment, and identify infants that are carriers of genes for certain diseases.