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Current research on thalassemia treatment focuses on several promising areas, including gene therapy, which aims to correct the genetic mutations responsible for the disorder. Clinical trials are exploring the use of CRISPR/Cas9 technology to edit genes and potentially provide a long-term cure. Additionally, advancements in stem cell transplantation and novel medications, such as small molecule therapies that enhance hemoglobin production, are being investigated to improve patient outcomes and reduce the need for blood transfusions. Overall, these innovative approaches hold the potential to significantly improve the quality of life for individuals with thalassemia.

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3w ago

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