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2,240 Possible Causes for Glycogen Storage Disease Type 1, Mean Corpuscular Volume Increased, 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.[] Reticulocyte counts are usually elevated, and an increased MCV (mean corpuscular volume) (greater than 100 fl) can be seen, due to the larger size of reticulocytes in comparison[] -Red cell morphology on review of the peripheral blood smear may demonstrate microspherocytes and polychromasia which are suggestive of a reactive reticulocytosis.[]

  • 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[] Tests include complete blood count (CBC) and peripheral smear.[] In cold agglutinin disease, RBCs clump on the peripheral smear, and automated cell counts often reveal an increased mean corpuscular volume and spuriously low hemoglobin due[]

  • Portal Cirrhosis

    Less common causes include genetic conditions such as hemochromatosis, cystic fibrosis, Wilson’s disease, biliary atresia, and glycogen storage disease.[] storage disease Tyrosinemia Wilson disease Alpha1-antitrypsin deficiency Cystic fibrosis Bile duct diseases: Biliary artresia Sclerosing cholangitis Congenital hepatic fibrosis[] storage disease) Genetic digestive disorder (Alagille syndrome) Liver disease caused by your body's immune system (autoimmune hepatitis) Destruction of the bile ducts (primary[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Congenital Dyserythropoietic Anemia

    Anisopoikilocytosis with tear-drop forms, polychromasia, basophilic stippling in peripheral blood smear, erythroid hyperplasia with megaloblastoid changes, binucleated cells[]

    Missing: Glycogen Storage Disease Type 1
  • Cold Agglutinin Disease

    Reticulocytes and Spherocytes The results of the reticulocyte count are usually increased in patients with cold agglutinin disease, with polychromasia in the peripheral blood[] blood smear : spherocytes , polychromasia Coombs test : positive Cold agglutinins titer C3 and C4 ; (due to complement activation) Prognosis: spontaneous remission within[] The mean corpuscular volume (MCV) is elevated because of reticulocytosis, as well as agglutination of the RBCs.[]

    Missing: Glycogen Storage Disease Type 1
  • Congenital Hemolytic Anemia

    Laboratory The review of the peripheral blood smear revealed no evidence of the schistocytes or fragmented red cells.[] Mean corpuscular hemoglobin concentration (MCHC) is increased (35-38%) in approximately 50% of patients.[] 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[]

    Missing: Glycogen Storage Disease Type 1
  • Gaucher Disease

    An autsomal recessive deficiency of acid Beta glucocerebrosidase most common glycogen storage disease 1 in 40,000 incidence most common in Ashkenazi Jewish origin what is[] Pompe Disease Infantile Pompe disease (IPD), also known as infantile acid maltase deficiency and type 2 glycogen storage disease, is an autosomal recessive muscle-wasting[] Enzyme replacement therapy with alglucosidase alfa in 44 patients with late-onset glycogen storage disease type 2: 12-month results of an observational clinical trial.[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Vitamin B12 Deficiency

    Hematological presentation of cobalamin deficiency ranges from the incidental increase of mean corpuscular volume and neutrophil hypersegmentation to symptoms due to severe[] Diagnostic methods Diagnosis depends on blood tests that show low serum levels of cobalamin and megaloblastic anemia (decreased red blood cell count and increased mean corpuscular[] corpuscular volume, MCV).[]

    Missing: Glycogen Storage Disease Type 1 Polychromasia in Peripheral Blood Smear
  • Subacute Combined Degeneration of Spinal Cord

    In glycogen-storage diseases glycogen cannot be metabolized to yield lactic acid and energy, so that it accumulates within muscle, liver, and other tissues.[] In the glycogen storage diseases glycogen accumulates in muscle fibre, because of a deficiency of an enzyme that helps degrade glycogen into lactic acid for the production[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Juvenile Myxedema

    storage disease McArdle's disease Pompe's disease von Gierke's disease 271.1 Galactosemia Galactose-1-phosphate uridyl transferase deficiency Galactosuria 271.2 Hereditary[] […] glucagon (251.4) diabetes mellitus (250.0-250.9) hypoglycemia NOS (251.2) mucopolysaccharidosis (277.5) 271.0 Glycogenosis Amylopectinosis Glucose-6-phosphatase deficiency Glycogen[]

    Missing: Polychromasia in Peripheral Blood Smear

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