Newborn disease screening

Newborn disease screening is a simple, fast, and inexpensive blood spot test that allows early detection of a child with a congenital genetic disease and timely treatment for healthy growth. Some congenital metabolic diseases, although the incidence is very low, can seriously affect mental development, and can lead to lifelong disability. No diagnosis can be made before birth, and there are no symptoms early after birth. However, once an abnormal condition occurs, the nervous system She has suffered irreversible damage and lost her treatment. Early detection, early detection and early treatment after birth can protect the child from damage and prevent mental retardation.

The material in this site is intended to be of general informational use and is not intended to constitute medical advice, probable diagnosis, or recommended treatments.