Newborn Screening

Newborn screening is a routine procedure used to test newborns for certain inherited metabolic and other disorders. These tests allow for the early detection of serious conditions that, if left untreated, can lead to permanent damage or death. The tests are conducted a few days after birth, usually involving a small blood sample taken from the baby's heel. In Croatia, newborn screening is routinely used to detect disorders such as phenylketonuria and congenital hypothyroidism.

The goal of screening is to ensure early intervention and treatment to prevent severe complications and enable normal child development. It is a safe and non-invasive procedure that can greatly improve the quality of life.