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54 Possible Causes for Congenital Hemolytic Anemia, Polychromasia in Peripheral Blood Smear

  • Congenital Dyserythropoietic Anemia Type 1

    She has long been diagnosed with unclassified congenital hemolytic anemia from the neonatal period.[ncbi.nlm.nih.gov] Anisopoikilocytosis with tear-drop forms, polychromasia, basophilic stippling in peripheral blood smear, erythroid hyperplasia with megaloblastoid changes, binucleated cells[unboundmedicine.com] E. 2018 10 Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia. ( 29936674 ) Hamada M....Kojima S. 2018 11 Fetal-onset[malacards.org]

  • Autoimmune Hemolytic Anemia

    […] from congenital hemolytic anemia.[en.wikipedia.org] Peripheral blood smear showed polychromasia and spherocytosis. Haptoglobin level was 0.06 g/L ( N 0.16-2). Both hemoglobin electrophoresis and G6PD level were normal.[jahjournal.org] -Red cell morphology on review of the peripheral blood smear may demonstrate microspherocytes and polychromasia which are suggestive of a reactive reticulocytosis.[oncologynurseadvisor.com]

  • Pyruvate Kinase Deficiency

    HEREDITARY spherocytosis with its associated congenital hemolytic anemia is generally easily recognized and satisfactorily treated with splenectomy.[nejm.org] Peripheral blood smear showed polychromasia, anisocytosis, tear drop cells, fragmented eyrtrocytes, and target cells.[ncbi.nlm.nih.gov] Pyruvate kinase deficiency is a rare cause of congenital hemolytic anemia.[ncbi.nlm.nih.gov]

  • Hemolytic Anemia

    A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.[icd9data.com] Mean corpuscular volume was 96 fl, and the reticulocyte count was 11%, with marked polychromasia on peripheral smear.[care.diabetesjournals.org] Congenital Hemolytic Anemia In congenital hemolytic anemias, the destruction of red blood cells is caused by a defect within the red blood cells themselves.[ucsfbenioffchildrens.org]

  • Congenital Dyserythropoietic Anemia

    She has long been diagnosed with unclassified congenital hemolytic anemia from the neonatal period.[ncbi.nlm.nih.gov] Anisopoikilocytosis with tear-drop forms, polychromasia, basophilic stippling in peripheral blood smear, erythroid hyperplasia with megaloblastoid changes, binucleated cells[ncbi.nlm.nih.gov] anemia congenital hemolytic anemia characterized by ineffective erythropoiesis, and resulting from a decrease in the number of red blood cells (RBCs) in the body and a less[wikidata.org]

  • Congenital Hemolytic Anemia

    Congenital hemolytic anemia refers to hemolytic anemia which is primarily due to congenital disorders.[en.wikipedia.org] Laboratory The review of the peripheral blood smear revealed no evidence of the schistocytes or fragmented red cells.[medcraveonline.com] blood smear of Congenital Hemolytic Anemia Describe the extent of central pallor of a normal RBC T/F: There is increased reticulocytosis and polychromasia in Congenital Hemolytic[brainscape.com]

  • Hemoglobin SC Disease

    Sickle and target cells, polychromasia, and sometimes Howell–Jolly bodies are detected on peripheral blood smears. Results of sickle cell solubility tests are positive.[clinchem.aaccjnls.org]

  • Acquired Hemolytic Anemia

    hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency, acquired hemolytic anemia and vitamin B12 deficiency induced megaloblastic anemia..[ncbi.nlm.nih.gov] blood smear : spherocytes, polychromasia Coombs test : positive Cold agglutinins titer C3 and C4 ; (due to complement activation) Prognosis: spontaneous remission within[amboss.com] hemolytic anemia causes (broad) membrane disorders enzyme disorders Hb disorders congenital hemolytic anemia MEMBRANE DISORDERS spherocytosis eliptocytosis congenital hemolytic[quizlet.com]

  • Congenital Heinz Body Hemolytic Anemia

    CHBHA stands for "Congenital Heinz Body Hemolytic Anemia" How to abbreviate Congenital Heinz Body Hemolytic Anemia?[allacronyms.com] The stained peripheral blood smear shows anisocytosis, poikilocytosis, basophilic stippling, polychromasia and, sometimes, hypochromia.[mayomedicallaboratories.com] Abstract The mechanisms of hemoglobin precipitation into Heinz bodies and hemolytic anemia that characterize congenital Heinz body hemolytic anemia (CHBHA) were studied in[ncbi.nlm.nih.gov]

  • Hemolytic Anemia due to a Disorder of Glycolytic Enzymes

    anemia and congenital hemolytic anemia.[malacards.org] blood smear : spherocytes, polychromasia Coombs test : positive Cold agglutinins titer C3 and C4 ; (due to complement activation) Prognosis: spontaneous remission within[amboss.com] , as an aid in searching Hereditary nonspherocytic hemolytic anemia Congenital hemolytic anemia Adenlyate kinase deficiency AK AK1 ALDOA Aldolase A deficiency ALDOA deficiency[mayomedicallaboratories.com]

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