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534 Possible Causes for Sickle Cell Trait, Thrombocytopenia

  • Sickle Cell Disease

    Patients should be monitored for leukopenia and thrombocytopenia. Complications from long-term usage are not yet known. Efficacy in children has not been proven.[] Is there a difference between sickle cell anemia and sickle cell trait? Yes.[] The commonest side effects included neutropenia and thrombocytopenia.[]

  • Red Blood Cell Disorder

    Numerous conditions cause thrombocytopenia; most do not result in abnormal bleeding.[] A person who has sickle cell trait usually expresses less than 40% HbS, and the client with sickle cell disease may express 85% to 95% HbS.[] Evaluations available include: Pancytopenia Leukopenia Thrombocytopenia (Auto) Immune thrombocytopenia (ITP) Drug-induced cytopenias (anemia, thrombocytopenia, leukopenia)[]

  • Posthemorrhagic Anaemia of the Newborn

    Dreyfus M, Kaplan C, Verdy E, Schlegel N, Duran-Zaleski I, Tchernia G; and the Immune Thrombocytopenia Working Group: Frequency of immune thrombocytopenia in newborns: a prospective[] (e.g., anemia of chronic disease, aplastic anemia ); an increased production of HbS as seen in sickle cell disease (not sickle cell trait); an increased destruction or loss[] […] hemoglobinopathy (282.60-282.69) that with thalassemia (282.49) 282.6 Sickle-cell disease Sickle-cell anemia Excludes: sickle-cell thalassemia (282.41-282.42) sickle-cell[]

  • Leukoerythroblastic Anemia

    Acute Erythroblastic Leukemia Anemia, X-Linked, without Thrombocytopenia aplastic anemia Aplastic Anemia, Idiopathic Bone Marrow Failure Syndromes chronic myeloid leukemia[] […] hemoglobinopathy (282.60-282.69) that with thalassemia (282.49) 282.6 Sickle-cell disease Sickle-cell anemia Excludes: sickle-cell thalassemia (282.41-282.42) sickle-cell[] […] who presented seven years following apparently successful surgery and adjuvant chemo-radio-therapy, with blood film findings of microangiopathic hemolytic anemia (MAHA), thrombocytopenia[]

  • Heat Stroke

    CONCLUSION: The high mortality observed in HS complicated with AKI, and among the various hematological parameters assessed, thrombocytopenia is associated with AKI induced[] cell trait.[] These include heart, lung, or kidney disease, obesity or underweight, high blood pressure, diabetes, mental illness, sickle cell trait, alcoholism, sunburn, and any conditions[]

  • Normocytic Normochromic Anemia

    B19, EBV, HIV, HCV - Fanconi's anemia: autosomal recessive disorder - Radiation - Benzene - Chloramphenicol (antibiotic) Aplastic anemia: features Pancytopenia - Anemia - Thrombocytopenia[] Which is the major Hgb found in the RBC's of patients with sickle cell trait? A. Hgb S B. Hgb F C. Hgb A2 D. Hgb A 8.[] In a patient with sickle cell trait, what are the relative amounts of hemoglobin one would expect to see in electrophoresis?[]

  • Aplastic Anemia

    After the initial appearance of AMI approximately 2 months earlier, he had received conservative treatment/transfusion alone because of severe thrombocytopenia and anemia[] Researchers have found that having sickle cell trait offers some survival advantage against malaria.[] In women, this can lead to menorrhagia secondary to thrombocytopenia which may require treatment depending on its severity.[]

  • Plasmodium Falciparum Malaria

    Statistics from Plasmodium falciparum malaria thrombocytopenia traveller Thrombocytopenia is frequent in patients with acute malaria and is sometimes profound[] However, people who have sickle cell trait (only one sickle cell gene) do not have the complications of sickle cell disease, but their hemoglobin is just abnormal enough to[] cell trait are less susceptible to P. falciparum malaria and persons who lack certain Duffy blood group determinants are protected against P. vivax infection Glucose-6-phosphate[]

  • Congenital Heinz Body Hemolytic Anemia

    Thrombocytopenia with absent radii (TAR) syndrome Excludes: Wiskott-Aldrich syndrome (279.12) 287.39 Other primary thrombocytopenia 287.4 Secondary thrombocytopenia Posttransfusion[] cell anemia, Sickle cell trait, Sickle hemoglobin, sickle trait, The Hemoglobinopathies Hemoglobin Structure Abnormalities Hemoglobin consists of one heme unit (a complex[] Blood film spherocytes (AIHA, hereditary spherocytosis) helmet cells blister cells (oxidative damage in G6PD deficiency) schistocytes (TTP or DIC with thrombocytopenia) or[]

  • Sickle Cell Crisis

    Thrombocytopenia is unusual in sickle cell disease.[] Sickle cell trait can never become sickle cell disease. It is possible, however, for individuals with sickle cell trait to pass the gene to their children.[] Laboratory findings included thrombocytopenia, microcytic anemia, and markedly elevated ferritin.[]

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