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

  • Autoimmune Hemolytic Anemia

    Laboratory investigations were suggestive of intravascular hemolysis, and on immuno-hematological evaluation it was diagnosed that the patient had autoantibody with mimicking[ncbi.nlm.nih.gov] 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] Exposure to cold led to worsening of the patient's hemolysis and hemoglobinuria.[ncbi.nlm.nih.gov]

  • Paroxysmal Cold Hemoglobinuria

    2015 ICD-9-CM Diagnosis Code 283.2 Hemoglobinuria due to hemolysis from external causes 2015 Billable Thru Sept 30/2015 Non-Billable On/After Oct 1/2015 ICD-9-CM 283.2 is[icd9data.com] 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]

  • Zieve's Syndrome

    Lab studies revealed hemolysis as the cause of anemia. The patient was diagnosed with Zieve's syndrome and managed with supportive measures.[doi.org] 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]

  • Hemolytic Anemia due to a Disorder of Glycolytic Enzymes

    […] birth, severe transfusion-dependent chronic hemolysis, moderate hemolysis with exacerbation during infection, to a fully compensated hemolysis without apparent anemia.[orpha.net] "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]

  • Pyruvate Kinase Deficiency

    We report here the case of a 1-year-old girl with mild hemolysis and PKD.[ncbi.nlm.nih.gov] 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] To our knowledge, the present case is the first described in which the same condition is associated with hemolysis.[ncbi.nlm.nih.gov]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    Acetaminophen was the most likely cause of the hemolysis. Clinicians must be aware of this potential complication after acetaminophen overdose in G6PD-deficient patients.[ncbi.nlm.nih.gov] 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]

  • Familial Pseudohyperkalemia

    The red blood cells show a reduced lifespan in vivo but there is no frank hemolysis.[moh-it.pure.elsevier.com] 1 - Hyperprolinemia - Sarcosinemia Carbohydrate Lactose intolerance - Glycogen storage disease ( type I , type II , type III, type IV, type V , type VI, type VII ) - fructose[bionity.com] Her peripheral blood smear revealed polychromasia, target cells, and a few spherocytes.[haematologica.org]

  • Erythropoietic Porphyria

    But, CEP without hemolysis is very rare.[doi.org] 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]

  • Anemia due to Glutathione Metabolism Disorder

    In acute hemolysis, reticulocytosis appears 5 days after hemolysis, maximum level reaches between 7-10 days, after which the levels decline.[medcaretips.com] […] deficiency GK Glycogen storage disease of heart (lethal) PRKAG2 Glycogen storage disease type 0 muscle GYS1 Glycogen storage disease type 0 GYS2 Glycogen storage disease[centogene.com] The peripheral blood smear post-splenectomy often shows crenated or spiculated spherocytes and marked polychromasia.[clinicaladvisor.com]

  • Chronic Acquired Pure Red Cell Aplasia

    Approach to normocytic anemia (Pure red cell aplasia check reticulocyte count normocytic anemia increased Is there evidence of hemolysis?[slideshare.net] 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]

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