North Carolina's newborn screening program receives federal grant

North Carolina will receive $1.7 million to support its newborn screening program. The money will be distributed to the North Carolina Department of Health and Human Services over five years.

The funding has been awarded from a division of the U.S. Health Resources and Services Administration. The goal is to improve and build upon advancements in the state’s newborn screening system.

Officials hope to enhance the early detection of genetic or biochemical disorders. The grant will also benefit follow-up programs for families seeking help navigating the treatment landscape.

Dr. Scott Shone, the director of the state Laboratory of Public Health, says the funding will be used to update data systems, expand educational outreach, and make improvements both in the lab and with follow-up procedures.

According to a news release, newborn blood tests detect rare genetic or biochemical disorders in over 200 babies in North Carolina every year. Studies support the importance of early identification and treatment.