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Sickle Cell Disease news and research updates

Research readouts, treatment and access decisions, and community updates for people living with sickle cell disease and the people who care for them — each one dated, with a link to the original source where there is one.

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  1. Not so benign: Life-threatening hematuria from renal papillary necrosis in sickle cell trait

    Highlights Sickle cell trait can cause severe, transfusion-dependent hematuria -- not always benign; requires thorough evaluation. Consider renal papillary necrosis for recurrent…

  2. Mandibular Osteomyelitis and Acute Soft Head Syndrome in an Adolescent With Sickle Cell Disease

    Abstract Sickle cell disease (SCD) is a type of inherited disorder of hemoglobin characterized by recurring vaso-occlusive pain crises that affect many organ systems. Although it…

  3. Sickle Cell Disease: Can genetic variability influence pregnancy outcomes?

    Abstract Pregnancy in Sickle Cell Disease (SCD), a severe hereditary genetic condition, highly prevalent in Sub-Saharan African countries, is associated with increased risk of…

  4. Orbital Compression Syndrome Mimicking Severe Malaria in a Child with Sickle Cell Disease in a Ugandan Refugee Settlement: A Case Report

    Orbital compression syndrome (OCS), also referred to in the sickle cell disease (SCD) literature as orbital infarction syndrome, is an uncommon but potentially sight-threatening…

  5. Oxygen Timing as Therapy: Molecular Rationale and Clinical Imperative for Early Oxygen Administration in the Sickle Cell Disease Vaso-Occlusive Crisis—A Structured Narrative Review with Implications for Resource-Constrained Health Systems

    Abstract Sickle cell disease (SCD) is a monogenic hemoglobinopathy in which hemoglobin S (HbS) polymerizes on deoxygenation, leading to sickling of red blood cells (RBCs) and…

  6. Impact of hydroxyurea use on severity and hematologic profile in children with sickle cell disease at University of Benin Teaching Hospital, Benin city, Nigeria

    Abstract Background: Sickle cell disease (SCD) is a major cause of morbidity and mortality among children in sub-Saharan African. Hydroxyurea (HU) remains the cornerstone of…

  7. Hydroxyurea treatment for sickle cell disease in Nairobi informal settlements: A retrospective cohort study

    Background: Sickle Cell Disease (SCD) causes acute and chronic complications. Hydroxyurea (HU) reduces vaso-occlusive crises (VOCs), and improves patients’ outcomes. However…

  8. Zydus Lifesciences Gets Green Light For Phase III Desidustat Trial In Sickle Cell Patients

    Zydus Lifesciences is advancing its clinical pipeline with permission to start Phase III clinical trials of Desidustat, an oral therapeutic candidate for Sickle Cell Disease. The…

  9. Colchicine Protects Against Sickle Cell Related Cardiomyopathy: Evidence of the Novel Role of Inflammaging

    Abstract Sickle cell disease (SCD) is a globally distributed hereditary red cell disorder with still high mortality. Growing evidence indicates that sickle cell related…

  10. Sickle Cell Disease Linked to Higher Postpartum LARC Use

    TOPLINE People with sickle cell disease (SCD) had 82% higher odds of receiving immediate postpartum long-acting reversible contraception (LARC) than those without SCD in a study…

  11. Sickle Cell Disease: From Ancient Origins to Modern Breakthroughs in Gene Therapy

    In the manuscript “Sickle Cell Disease: From Ancient Origins to Modern Break-2 throughs in Gene Therapy” by Drs. Bawo Ikolo et al, the authors examine various aspects of sickle…