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Sickle Cell Anemia SCA Action Plan over Revised 32709 All Current Medications Name of Medication Dosage Time Medication to Be Gi  Form

Sickle Cell Anemia SCA Action Plan over Revised 32709 All Current Medications Name of Medication Dosage Time Medication to Be Gi Form

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in a study published in the New England Journal of Medicine three patients with severe sickle cell disease were treated with a new Gene editing tool called crispr cast 9. this treatment led to an increase in the healthy fetal hemoglobin in their bodies replacing the harmful sickle hemoglobin that causes the disease the treatment was successful in all three patients with no side effects and resulted in improved health over a period of 6 to 18 months

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