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381 Possible Causes for Sickle Cell Disease, Thrombocytosis

  • Pulmonary Embolism

    cell anemia, thrombocytosis, dehydration,, advanced age, cancer, and obesity.[] […] contraceptives, postmenopausal hormones, atrial fibrillation, vascular injury, IV drug abuse, polycythemia vera, heart failure, autoimmune hemolytic anemia, sickle cell anemia, thrombocytosis[] Diagnosis is challenging because symptoms are nonspecific and often misinterpreted and may mimic other diseases of the limbs, abdomen, or chest.[]

  • Splenic Infarction

    Splenic infarction can also result from a sickle cell crisis in patients with sickle cell anemia.[] Changes in the blood count included anemia (53%), leukocytosis (49%), and thrombocytosis (7%).[] Hayag-Barin JE, Smith RE, Tucker FC Jr (1998) Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: a case report and review of the literature.[]

  • Sickle Cell Disease

    KEYWORDS: Acute chest syndrome; acute sickle cell crisis; emergencies in sickle cell disease; respiratory failure in sickle cell disease[] sickle cell disease but does not have sickle cell disease themselves.[] Treatment for a sickle cell crisis includes: Blood transfusions (may also be given regularly to prevent stroke) Pain medicines Plenty of fluids Other treatments for sickle[]

  • Spleen Disease

    Sickle Cell Disease Spleen Complications Normally, flexible and smooth red blood cells pass swiftly through the spleen.[] […] marrow, such as the spleen and liver) Thrombosis and thrombohemorrhagic complications (blood clotting or bleeding complications) Leukocytosis (too many white blood cells) Thrombocytosis[] A person with sickle cell disease makes a different kind of hemoglobin called sickle hemoglobin.[]

  • Congenital Hemolytic Anemia

    cell disease?[] […] coagulability primary: Antithrombin III deficiency · Protein C deficiency / Activated protein C resistance / Protein S deficiency / Factor V Leiden · Hyperprothrombinemia acquired: Thrombocytosis[] Laboratory studies (Table 1 ) showed severe microcytic and hypochromic anemia with reticulocytopenia, a normal white blood cell count and thrombocytosis.[]

  • Iron Deficiency

    When a specific gene is damaged, for example, an abnormal protein or lack of protein can cause disease such as hemophilia or sickle cell disease.[] OBJECTIVE: In order to inquire into the pathogenesis of increased platelet counts in peripheral blood of patients with iron deficiency anemia (IDA), the phenomenon of thrombocytosis[] Sickle cell anemia Causes: Inherited disease that is most common among African-Americans; red blood cells become sickle-shaped Factors: Hemoglobin doesn't work right; the[]

  • Cooley's Anemia

    Come here and be informed about Cooley’s Anemia (Thalassemia) and Sickle Cell Disease! Organizer Queens Sickle Cell Advocacy Network, Inc.[] Complications of splenectomy including sepsis and thrombocytosis should be noted and prevented.[] Essential Thrombocytosis – A disorder in which platelets are overproduced, which can lead to both blood clotting and bleeding.[]

  • Iron Deficiency Anemia

    cell disease Thalassemia Why Choose the Hematology Program?[] OBJECTIVE: In order to inquire into the pathogenesis of increased platelet counts in peripheral blood of patients with iron deficiency anemia (IDA), the phenomenon of thrombocytosis[] […] inherited blood disorders, such as sickle cell disease or thalassemia.[]

  • Hereditary Spherocytosis

    Hereditary spherocytosis (HS) and sickle cell disease (SCD) are associated with splenomegaly and spleen dysfunction in pediatric patients.[] It also results in leukocytosis and thrombocytosis. On peripheral blood smear, spherocytes are unchanged or may even increase.[] cell disease and hereditary spherocytosis The identification of the ferroportin/hepcidin axis has allowed the effect of erythroid activity on iron balance to be studied and[]

  • Nephrotic Syndrome

    disease (SCD).[] Antiplatelet therapy was instituted with dipyridamole to prevent thromboembolism from the combination of nephrotic syndrome and thrombocytosis.[] Unlike QMN, hepatitis B virus, HIV infection, sickle cell disease and systemic lupus erythematosus are now increasingly being associated with NS in TpAfr.[]

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