Create issue ticket

150 Possible Causes for Anemia, Anisopoikilocytosis

Show results in: Italiano

  • Thalassemia

    Beta-thalassemia and sickle cell anemia are two of the most common diseases related to the hemoglobin protein.[] Blood analysis shows reduced Hb levels ( 7 g/dl), mean corpuscular volume (MCV) 50 70 fl, and mean corpuscular Hb (MCH) 12 20 pg, anisopoikilocytosis and presence of erythroblasts[] Peripheral smear shows target cells, teardrop RBCs, polychromasia, moderate anisopoikilocytosis, and basophilic stippling.[]

  • Myelodysplasia

    Who has aplastic anemia and MDS?[] Red cell morphology in the peripheral blood may be normal or macrocytic with anisopoikilocytosis.[] Aplastic Anemia and Myelodysplasia Association of Canada The Aplastic Anemia & Myelodysplasia Association of Canada (AAMAC) is a volunteer-run organization supporting patients[]

  • Sideroblastic Anemia

    anemia.[] Showing marked anisopoikilocytosis, basophilic stippling, polychromasia and nRBCs.[] […] groups: congenital sideroblastic anemia, acquired clonal sideroblastic anemia, and acquired reversible sideroblastic anemia.[]

  • Iron Deficiency Anemia

    Iron deficiency anemia is a common type of anemia, affecting millions of people worldwide. Iron deficiency anemia is often asymptomatic.[] A sufficiently low hemoglobin (Hb) by definition makes the diagnosis of anemia, and a low hematocrit value is also characteristic of anemia.[] Iron deficiency is one of the most common causes of anemia.[]

  • Megaloblastic Anemia

    The present study aimed to assess the relation between obesity parameters and the occurrence of iron deficiency anemia and also megaloblastic anemia among Iranian population[] [ macrocytosis is the earliest sign in Vit B12 deficiency and can be detected even before the onset of anaemia ] - In severe anaemia in addition to macrocytosis, marked anisopoikilocytosis[] Megaloblastic anemia has a rather slow onset, especially when compared to that of other anemias.[]

  • Congenital Hemolytic Anemia

    ICD - 9-CM 282 MeSH D000745 [ edit on Wikidata ] Congenital hemolytic anemia (or hereditary hemolytic anemia ) refers to hemolytic anemia which is primarily due to congenital[] Hereditary pyropoikilocytosis is an inherited red cell membrane disorder with characteristic morphology: striking anisopoikilocytosis with red cell fragmentation and microspherocytes[] Description Hereditary pyropoikilocytosis (HPP) is a recessively inherited form of hemolytic anemia characterized by peripheral blood morphology presenting with striking anisopoikilocytosis[]

  • Congenital Dyserythropoietic Anemia

    anemia resulting in cardiac failure and relatively mild dyserythropoietic features on bone marrow aspiration in contrast to severity of anemia.[] Anisopoikilocytosis with tear-drop forms, polychromasia, basophilic stippling in peripheral blood smear, erythroid hyperplasia with megaloblastoid changes, binucleated cells[] […] and hallux varus deformity of the great toe of the right foot was diagnosed to have congenital dyserythropoietic anemia on the basis of the hematological (macrocytosis, anisopoikilocytosis[]

  • Pancytopenia

    Pancytopenia is most commonly seen in aplastic anemia. In aplastic anemia, our immune system attacks the healthy cells of bone marrow.[] MCV values 100fL and 110fL were more frequent in patients with megaloblastic anemia with most prominent anisopoikilocytosis, microcytosis and fragmented RBCs.[] A blood film showed marked anaemia with red cell anisopoikilocytosis, prominent tear drop cells and neutropenia with normal white cell morphology.[]

  • Hereditary Elliptocytosis

    Auto-immune haemolytic anemia complicating infectious mononucleosis occurred in a patient with hereditary elliptocytosis.[] Hereditary pyropoikilocytosis (HPP) is a severe, congenital hemolytic anemia occurring almost exclusively in black persons and characterized by extreme red blood cell anisopoikilocytosis[] Hereditary spherocytosis is the most common cause of hemolytic anemia among people of Northern European descent.[]

  • Alkylating Agent

    The mRNA encoding the major bcr/abl fusion protein then appeared in the stage of sideroblastic anemia.[] […] sideroblasts common; 5% myeloblasts Microscopic (histologic) images Images hosted on PathOut server: Peripheral blood: Postchemotherapy for breast cancer, erythrocytes have anisopoikilocytosis[] Chromosome instability is known to be associated with certain autosomal recessive cancer-prone disorders such as Fanconi's anemia.[]

Further symptoms

Similar symptoms