Each year, the New York State Department of Health screens more than 205,000 newborns for over 50 rare but serious conditions. These include metabolic and endocrine disorders, hemoglobinopathies, infectious diseases, and other genetic disorders. Early detection through this program allows for timely treatment that can prevent severe illness, developmental delays, or death.
In 2024, the screening program identified 671 infants with one of the conditions on its panel. Since its start in 1965, the program has tested over 10 million infants across New York State.
State Health Commissioner Dr. James McDonald said, “Newborn screening is one of the most important tools we have to protect children’s health from the very beginning. By identifying conditions early, we can ensure babies receive the specialized care they need to grow and thrive.”
The New York State Newborn Screening Program is recognized nationally for its innovation. It continues to improve existing screenings, pilot new tests for additional conditions, and expand its panel based on updated recommendations. The program works closely with hospitals, pediatricians, and families to provide follow-up testing as well as counseling and support services when needed.
More information about the New York State Newborn Screening Program can be found here.
