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1,840 Possible Causes for Glycogen Storage Disease Type 1, Osmotic Fragility 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.[] Red blood cell agglutination, polychromasia, target cells and spherocytes were seen on a peripheral smear.[]

  • Glycogen Storage Disease Type 1

    Author information 1 Beatrix Children's Hospital, Groningen, The Netherlands. Abstract Life expectancy in glycogen storage disease type 1 (GSD-1) has[] OBJECTIVE: To study endocrine and metabolic variables that affect growth in patients with glycogen storage disease type 1 (GSD-1) receiving standard dietary therapy.[] Glycogen storage disease type 1 (GSD1) is an inborn error of metabolism caused by deficiency of glucose-6-phosphatase, the enzyme catalysing the conversion of glucose-6-phosphate[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Congenital Hemolytic Anemia

    Laboratory The review of the peripheral blood smear revealed no evidence of the schistocytes or fragmented red cells.[] Osmotic fragility of fresh blood was increased, and postsplenectomy blood showed a fraction of extremely fragile cells.[] The Type I cases showed the following features: normocytic or slightly macrocytic anemia with mild hypochromia and some stippling; a decreased or normal osmotic fragility[]

  • Anemia due to Glutathione Metabolism Disorder

    Cori's Disease (Glycogen Storage Disease Type III) Glycogen Storage Disease Autosomal Recessive.[] The peripheral blood smear post-splenectomy often shows crenated or spiculated spherocytes and marked polychromasia.[] Von Gierke's Disease (Glycogen Storage Disease Type I) Glycogen Storage Disease Autosomal Recessive.[]

  • Malaria

    BACKGROUND: Mobile populations and migrant workers are a key population to containing the spread of artemisinin-resistant malaria found in the border areas between Cambodia, Myanmar, and Thailand. Migrants often have limited knowledge of public health, including malaria, services in the area, and many seek care from[…][]

    Missing: Polychromasia in Peripheral Blood Smear
  • Normocytic Normochromic Anemia

    Peripheral blood smear shows: Microcytosis and hypochromasia. There is anisocytosis, poikilocytosis. There are pencil cells (elliptical RBCs).[] Normal MCV 80-100 fL/cell Normal MCHC Does hereditary spherocytosis increase osmotic fragility?[] There is polychromasia. Polychromasia in Hemolytic anemia Iron deficiency Anemia findings are: Low hemoglobin. Low Ferritin. Low serum iron. Low transferrin.[]

  • Glycogen Storage Disease Type 7

    Causes The disease, the same with glycogen storage diseases types 1 to 5, are caused by its autosomal recessive nature.[] Erythrocytes from the whippets were less osmotically fragile but more alkaline fragile than those from control dogs.[] Discuss Glycogen storage disease type 7 in our forums Discuss Glycogen storage disease type 7 with other members of Medigest in our forums.[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Hemoglobin C 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.[]

    Missing: Glycogen Storage Disease Type 1
  • Third Trimester Pregnancy

    OBJECTIVES: Characterise the demographics, management and outcomes of obstetric patients transported by emergency medical services (EMS). DESIGN: Prospective observational study. SETTING: Five Indian states using a centralised EMS agency that transported 3.1 million pregnant women in 2014. PARTICIPANTS: This study[…][]

    Missing: Glycogen Storage Disease Type 1 Polychromasia in Peripheral Blood Smear
  • 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".[] blood smear : spherocytes, polychromasia Coombs test : positive Cold agglutinins titer C3 and C4 ; (due to complement activation) Prognosis: spontaneous remission within[] Haemoglobin electrophoresis and red cell osmotic fragility are normal. Indirect hyperbilirubinaemia reflects the severity of the haemolytic process.[]

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