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185 Possible Causes for Mild Anemia, Reticulocyte Count Decreased

  • Iron Deficiency Anemia

    However, after subgroup analysis (degree of anemia), no significant difference in hemoglobin levels were found between both groups in mild anemia (mean difference 0.80; 95%[] Normal 0.5-1.5% Hypoprolifearative: Decreased reticulocytes Bone marrow unable to produce requisite number of RBC's Lack of essential substance (iron, B12, folate) or invasion[] People with mild anemia may not have any symptoms or may have only mild symptoms.[]

  • Alpha Thalassemia

    The heterozygous form may be asymptomatic or marked by mild anemia. β-thalassemia ( beta-thalassemia ) that caused by diminished synthesis of beta chains of hemoglobin.[] Reticulocytes, LDH and bilirubin are increased; haptoglobin is decreased.[] Alpha thalassemia causes mild anemia and is found in many ethnic groups. Usually it is found in regions where malaria is endemic.[]

  • Chronic Alcoholism

    […] before anemia develops.[] HEME – Megaloblastic anemia from folate deficiency.[] Alcoholism can also cause mild macrocytosis independent of folate deficiency, due to a direct effect on the bone marrow (common: 90% of alcoholics have MCV of 100-110 even[]

  • Aplastic Anemia

    Some people with aplastic anemia show no symptoms at all. Aplastic Anemia Treatment Patients with mild aplastic anemia that is not worsening may not need treatment.[] For example, for a person with anemia, an inappropriately low reticulocyte count often indicates decrease in red blood cell production in the bone marrow.[] Aplastic anemia can be mild, moderate or severe. Mild or moderate aplastic anemia is serious but usually does not require a stay in the hospital.[]

  • Anemia

    Even mild anemia may cause increased heart rate and affect left ventricular diastolic functions.[] A normal reticulocyte count confirms that the infant's bone marrow is functional.[] There are many types and causes of anemia. Mild anemia is a common and treatable condition that can occur in anyone.[]

  • Hereditary Elliptocytosis

    The patient presented for a general check up when his CBC showed only mild anemia with slightly increased reticulocytes.[] Hematological values showed an increase in reticulocyte counts and mean corpuscular hemoglobin concentration, decreased mean corpuscular volume and hematocrit, and normal[] Post-splenectomy, patients with HE or HPP exhibit increased hematocrit, decreased reticulocyte counts, and improved clinical symptoms.[]

  • Pernicious Anemia

    People with mild anemia may have no symptoms or very mild symptoms.[] Values obtained before treatment with cyanocobalamin were compared with those found during peak reticulocyte count.[] Response should be monitored by reticulocyte counts, lactic dehydrogenase (LDH), and an appropriate rise in hemoglobin levels.[]

  • Sideroblastic Anemia

    The proband's brother, an ALAS2 R452H hemizygote, had mild anemia and mild iron overload.[] RBC indices reveal a decreased MCV, MCH, and a decreased reticulocyte count which correlates with Iron deficiency anemia.[] A 62 year old male (R.H.) presented with a mild anemia (Hb 11-12 gm%) and a history of multiple hemorrhagic episodes. The marrow had 40-50% sideroblasts.[]

  • Leukoerythroblastic Anemia

    Mild anemias generally produce no symptoms but more severe anemia can cause shortness of breath, fatigue, and dizziness.[] Decreased count - reticulocyte levels drop where there is marrow infiltration (leukaemia, myeloma, lymphoma or other malignancies) or due to marrow underactivity such as in[] count- increased (10-15%) after 5-7 days Platelets- increased platelet production Stem cell suppression (environmental insult) causes genetically altered stem cell (express[]

  • Primary Myelofibrosis

    In pre-fibrotic PMF, patients typically present with mild anemia, mild granulocytosis, and thrombocytosis.[] , and polychromatophilia and very elevated reticulocyte counts can occur. 263,264 The antiglobulin (Coombs) test usually is negative, but red cell autoantibodies can develop[] It is characterized, classically, by anemia, mild neutrophilia, thrombocytosis, and splenomegaly. Occasional cases may present with bi- or tricytopenias ( 10%).[]

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