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17 Possible Causes for Glycogen Storage Disease Type 1, Polychromasia in Peripheral Blood Smear

  • Autoimmune Hemolytic Anemia

    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 blood cell agglutination, polychromasia, target cells and spherocytes were seen on a peripheral smear.[doi.org]

  • Normocytic Normochromic Anemia

    Peripheral blood smear shows: Microcytosis and hypochromasia. There is anisocytosis, poikilocytosis. There are pencil cells (elliptical RBCs).[labpedia.net] There is polychromasia. Polychromasia in Hemolytic anemia Iron deficiency Anemia findings are: Low hemoglobin. Low Ferritin. Low serum iron. Low transferrin.[labpedia.net]

  • Congenital Hemolytic Anemia

    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] Hemosiderinuria is seen in chronic intravascular hemolysis. 4) Examination of blood smear: Careful examination of peripheral blood smear by an experienced person provides[bioline.org.br]

  • Paroxysmal Cold Hemoglobinuria

    storage disease グリコーゲン蓄積症,糖原病(0a型) glycogen storage disease (type 0a) グリコーゲン蓄積症,糖原病(0b型) glycogen storage disease (type 0b) グリコーゲン蓄積症,糖原病(I型) glycogen storage disease (type[jsge.or.jp] Tests include complete blood count (CBC) and peripheral smear.[emedicine.com] The complete blood count usually shows normocytic anemia. Reticulocytosis may be subtle in the acute phase. Peripheral blood smear may show corresponding polychromasia.[en.wikipedia.org]

  • Zieve's Syndrome

    storage disease グリコーゲン蓄積症,糖原病(0a型) glycogen storage disease (type 0a) グリコーゲン蓄積症,糖原病(0b型) glycogen storage disease (type 0b) グリコーゲン蓄積症,糖原病(I型) glycogen storage disease (type[jsge.or.jp] The peripheral blood smear revealed polychromasia and nucleated erythrocytes. The parents’ blood counts and smears were normal.[indianpediatrics.net] The patient's peripheral smear showed polychromasia, macrocytosis, tear drop cells, ovalocytes, spur cells, and schistocytes ( Figure 1 ).[ncbi.nlm.nih.gov]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    In PFK deficiency (glycogen storage disease type VII), clinical hallmarks are male predominance with early onset gout, compensated hemolytic process, and prominent myopathy[ommbid.mhmedical.com] The peripheral blood smear showed polychromasia, anisopoikilocytosis and reticulocytosis (the reticulocyte count was 14.6%). Urine was positive for hemoglobinuria.[ncbi.nlm.nih.gov]

  • Chronic Acquired Pure Red Cell Aplasia

    storage disease グリコーゲン蓄積症,糖原病(0a型) glycogen storage disease (type 0a) グリコーゲン蓄積症,糖原病(0b型) glycogen storage disease (type 0b) グリコーゲン蓄積症,糖原病(I型) glycogen storage disease (type[jsge.or.jp] blood smear showed anisocytosis, poikilocytosis, polychromasia and leukocytosis.[ijmstrust.in] 型) glycogen storage disease (type IX) グリコーゲン蓄積症,糖原病(X型) glycogen storage disease (type X) グリコーゲン蓄積症,糖原病(XI型) glycogen storage disease (type XI) グリコーゲン蓄積症,糖原病(XII型) glycogen[jsge.or.jp]

  • Hemolytic Anemia due to a Disorder of Glycolytic Enzymes

    "Glycogen storage disease type I: diagnosis, management, clinical course and outcome.Results of the European study on glycogen storage disease type I".[cancertherapyadvisor.com] blood smear : spherocytes, polychromasia Coombs test : positive Cold agglutinins titer C3 and C4 ; (due to complement activation) Prognosis: spontaneous remission within[amboss.com] The peripheral blood smear post-splenectomy often shows crenated or spiculated spherocytes and marked polychromasia.[clinicaladvisor.com]

  • Erythropoietic Porphyria

    storage disease グリコーゲン蓄積症,糖原病(0a型) glycogen storage disease (type 0a) グリコーゲン蓄積症,糖原病(0b型) glycogen storage disease (type 0b) グリコーゲン蓄積症,糖原病(I型) glycogen storage disease (type[jsge.or.jp] A peripheral blood smear showed poikilocytosis, polychromasia, tear-drop cells, and normoblasts.[bloodjournal.org] 型) glycogen storage disease (type IX) グリコーゲン蓄積症,糖原病(X型) glycogen storage disease (type X) グリコーゲン蓄積症,糖原病(XI型) glycogen storage disease (type XI) グリコーゲン蓄積症,糖原病(XII型) glycogen[jsge.or.jp]

  • Retinitis pigmentosa, Y-Linked

    , Phospoglycerate kinase 1 deficiency form of Glycogen storage disease, Hunter’s syndrome, G6PD deficiency, HGPRT deficiency, OTC deficiency Most of the inherited inmmunodeficiencies[epomedicine.com] Peripheral smear revealed red blood cells with mild degree of anisocytosis, poikilocytosis, polychromasia with hypochromic, macrocytic RBCs, target cells and sickle cells.[ijo.in] Storage Disease Type VI 3 Glycogen Storage Disease Type VII 4 Glycogen Storage Disease Type X 3 Glycogen Storage Disease Type XI 2 Glycogen Storage Disease Type XII 2 Glycogen[preventiongenetics.com]

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