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3,279 Possible Causes for Exertional Dyspnea, 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.[] The disease is characterized by symptoms due to the anemia including fatigue, exertional dyspnea, and, more rarely, jaundice and dark urine in case of severe hemolysis.[] -Red cell morphology on review of the peripheral blood smear may demonstrate microspherocytes and polychromasia which are suggestive of a reactive reticulocytosis.[]

  • Cardiomyopathy

    dyspnea , a feeling of pressure in the chest Later stages Progressive left heart failure and right heart failure Relative mitral valve regurgitation Diagnostics Patient history[] storage disease Restrictive cardiomyopathy with endomyocardial fibrosis Restrictive cardiomyopathy without endomyocardial fibrosis Reversible myocardial perfusion defect[] storage disease; familial hypertrophic cardiomyopathy 6 ?[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Hypertrophic Cardiomyopathy

    A 10-month female infant who experienced cough, fever, aggressive exertional dyspnea, and recurrent cyanosis was admitted to our hospital.[] Adults with increased left ventricular thickness secondary to diseases such as amyloidosis and glycogen storage disease are usually excluded from the definition.[] Treatment strategies depend on appropriate patient selection, including drug treatment for exertional dyspnea (beta-blockers, verapamil, disopyramide) and the septal myotomy-myectomy[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Restrictive Cardiomyopathy

    dyspnea and palpitations.[] storage diseases idiopathic Plain radiograph The heart size can be normal.[] It usually manifests as a progressive heart failure with fatigue, exertional dyspnea and edema.[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Pulmonary Hypertension

    1 glycogen storage disease, Gaucher’s disease, hereditary hemorrhagic telangiectasia, hemoglobinopathies, myeloproliferative disorders, and splenectomy[] A 58-year-old woman was referred to our hospital with a chief complaint of exertional dyspnea.[] Common presenting features are exertional dyspnea, lethargy, fatigue, exertional syncope and chest pain, peripheral edema, anorexia and right upper quadrant pain.[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Dilated Cardiomyopathy

    Left ventricular dysfunction causes exertional dyspnea and fatigue due to elevated left ventricular diastolic pressure and low cardiac output.[] , cyclophosphamide, chloroquine, iron overload Endocrine diseases Hypothyroidism, hyperthyroidism, hypoparathyroidism, pheochromocytoma, hypoglycemia Metabolic disorders Glycogen-storage[] storage disease Sarcoidosis Chronic Chagas' cardiomyopathy HIV infection Other infectious disease - eg, adenovirus, Coxsackievirus, cytomegalovirus, toxoplasmosis, Lyme disease[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Cor Pulmonale

    storage disease Tumors pressing against pulmonary arteries Eisenmenger syndrome and pulmonary hypertension Eisenmenger syndrome, a type of congenital heart disease, causes[] The patient developed progressive exertional dyspnea, with clinical and laboratory findings of right-sided heart failure and pulmonary hypertension.[] Nonspecific: fatigue, tachypnea, exertional dyspnea, cough, anginal chest pain, hemoptysis, hoarseness What nonspecific signs may indicate underlying lung disease Increase[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Hemochromatosis

    A woman in her 70s was admitted with progressive dyspnea on exertion.[] […] variant in the BCS1L gene; relevant for Finnish descent Gaucher Disease Type 1 3 variants in the GBA gene; relevant for Ashkenazi Jewish descent Glycogen Storage Disease Type[] Ia 1 variant in the G6PC gene; relevant for Ashkenazi Jewish descent Glycogen Storage Disease Type Ib 2 variants in the SLC37A4 gene Hereditary Fructose Intolerance 4 variants[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Pulmonary Fibrosis

    A 71-year-old man developed exertional dyspnea and was diagnosed with IPF.[] storage disease (Gaucher’s), secondary pulmonary hypertension, and advanced stage sarcoidosis and others.[] The most pronounced clinical feature of pulmonary fibrosis is progressive exertional dyspnea associated with the production of dry cough.[]

    Missing: Polychromasia in Peripheral Blood Smear
  • Glycogen Storage Disease Type 1

    The main presenting symptoms are exercise intolerance, exertional dyspnea and congestive heart failure in progressed cases.[] 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[] Glycogen storage disease type 1 (GSD 1), also known as von Gierke's disease or Glycogen storage disease due to G6P deficiency, is the most common of the glycogen storage diseases[]

    Missing: Polychromasia in Peripheral Blood Smear

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