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North Carolina Sickle Cell Syndrome Program

1929 Mail Service Center
Raleigh, North Carolina, United States
Email   Phone   Web  

The mission of the North Carolina Sickle Cell Syndrome Program is to promote the health and well-being of persons with sickle cell disease through the reduction of morbidity and mortality and the heightened awareness of the disease and its complications. The program provides comprehensive services to individuals and their families affected by sickle cell disease and other hemoglobin disorders, and offers genetic counseling and education to the general public. Through the implementation of a systematic, statewide approach to service delivery, the program provides infants, children, adolescents and adults affected by sickle cell disease with newborn screening follow up, care coordination, referrals to clinical and related services, and sickle cell educational materials and information.

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