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Course Title CRISPR-Based Gene Therapy for the Induction of Fetal Hemoglobin in Sickle Cell Disease
Presented Date 02/27/2025
Expiration Date 02/27/2028
Presenter(s) Haydar Frangoul, M.D., MS
This Presenter does not have any relevant Financial Relationships to disclose.
This activity was not supported by an education grant or any in-kind support.

The Medical University of South Carolina designates this enduring material for a maximum of 1.0 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Description This is an online grand round from the Department of Medicine
Haydar Frangoul, M.D., MS Director of Pediatric Hematology/Oncology and Stem Cell Transplant, Sarah Cannon Research Institute at TriStar Centennial Children’s Hospital
Objectives Recognize the role of persistence of fetal hemoglobin in sickle cell disease; How does CRISPR gene editing work to modify hematopoietic stem cells; identify results of gene editing to induce fetal hemoglobin in individuals with sickle cell disease
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