Sickle Cell Disease (SCD)

Sickle Cell Disease (SCD) research and management focus on this inherited blood disorder characterized by abnormal hemoglobin. Recent advancements include disease-modifying therapies, gene editing trials, and improved pain management techniques. The field strives to enhance the quality of life for SCD patients by reducing complications, minimizing pain crises, and preventing organ damage. Additionally, prenatal testing and counseling aid in early diagnosis and family planning. SCD research is committed to finding curative solutions and alleviating the impact of this condition on affected individuals and their families.

  • SCD treatments and complications.
  • Advances in SCD research.
  • Strategies for improving SCD care.

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