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10 Possible Causes for Erythrocyte Morphology - Spherocytosis

  • Hereditary Spherocytosis

    DISORDER MEMBRANE DEFECT ABNORMAL MEMBRANE FUNCTION ERYTHROCYTE MORPHOLOGY HEREDITARY SPHEROCYTOSIS PRIMARY 50% ankirin DEFECIENCY SECONDARY band 3, then spectrin and other[slideshare.net] Assessment of total, direct, and indirect serum bilirubin, erythrocyte morphology and red cell characteristics (particularly mean corpuscular volume and mean sphered corpuscular[ncbi.nlm.nih.gov] Mild and moderate hereditary spherocytosis can be easily misdiagnosed.[ncbi.nlm.nih.gov]

  • Paroxysmal Cold Hemoglobinuria

    Other morphological abnormalities may be observed in the red blood cells such as poikilocytosis, polychromasia, spherocytosis, and nucleated erythrocytes.[symptoma.com]

  • Rh Deficiency Syndrome

    […] have a stomatocytosis & spherocytosis morphology increased erythrocyte osmotic fragility More General Terms hemolytic anemia Internet Database OMIM: 268150 References UniProt[anvita.info] […] phospholipid organization Genetics associated with defects in RHAG Clinical-manifestations chronic hemolytic anemia Laboratory complete blood count ( CBC ) peripheral blood smear : erythrocytes[anvita.info]

  • Pyruvate Kinase Deficiency

    Diseases Platelet Morphology, the Circulating Platelet Pre - cipitation of proteins by vinblastine and calcium ions[semanticscholar.org] Showing 1-10 of 19 references Cyclic nucleotide - membrane protein interaction in the regulation of erythrocyte shape and survival : Defect in hereditary spherocytosis , in[semanticscholar.org] Brewer Gi ( ed ) : Erythrocyte Structure and Function iL: Erythrocyte deformation in human muscular dystrophy Neurological Symptoms in Anemia, Neurological Symptoms in Blood[semanticscholar.org]

  • Hereditary Cryohydrocytosis with Reduced Stomatin

    The word 'stomatocyte' was first coined by Lock, Sephton-Smith and Hardisty14 at Great Ormond Street Hospital, London, to describe the erythrocyte morphology in a pale, jaundiced[the-medical-dictionary.com] In all other respects, it was identical to hereditary spherocytosis, except in the morphology, which showed a boat- or mouth-shaped red cell with a central slit of pallor[the-medical-dictionary.com]

  • Familial Pseudohyperkalemia

    The word 'stomatocyte' was first coined by Lock, Sephton-Smith and Hardisty14 at Great Ormond Street Hospital, London, to describe the erythrocyte morphology in a pale, jaundiced[the-medical-dictionary.com] In all other respects, it was identical to hereditary spherocytosis, except in the morphology, which showed a boat- or mouth-shaped red cell with a central slit of pallor[the-medical-dictionary.com]

  • Chronic Congestive Splenomegaly

    Trapping of erythrocytes in red pulp sinusoids Produces congestive splenomegaly Causes include: Abnormal RBC morphology (especially hereditary spherocytosis, thalassemias,[faculty.washington.edu]

  • Hereditary Elliptocytosis

    Mutations in 4.1R can cause hereditary elliptocytosis , a disease characterized by a loss of the normal discoid morphology of erythrocytes , resulting in hemolytic anemia[wikigenes.org] Hereditary spherocytosis , hereditary elliptocytosis or poikilocytosis, Southeast Asian ovalocytosis are hereditary hemolytic anemias , due to mutations in the genes encoding[wikigenes.org] […] conversion of spectrin dimers to tetramers result in hereditary elliptocytosis (HE), whereas a deficiency of human erythroid alpha- or beta-spectrin results in hereditary spherocytosis[wikigenes.org]

  • Hereditary Cryohydrocytosis with Normal Stomatin

    MEMBRANE DEFECTS Disorder Inheritance Pattern Membrane Defect Abnormal membrane function Erythrocyte Morphology Hereditary spherocytosis Usually-autosomal dominant rarely[sites.google.com] The word 'stomatocyte' was first coined by Lock, Sephton-Smith and Hardisty14 at Great Ormond Street Hospital, London, to describe the erythrocyte morphology in a pale, jaundiced[the-medical-dictionary.com] 3 · Spectrin structure Horizontal interaction defects (Produce elliptocytosis & other bizarre forms) · Actin · Protein 4.1 · Adductin · HEMOLYTIC ANEMIAS ASSOCIATED WITH ERYTHROCYTE[sites.google.com]

  • Hereditary Pyropoikilocytosis

    morphology similar to that seen in thermal burns.[translate.academic.ru] Patients with HPP tend to experience severe haemolysis… … Wikipedia Hereditary spherocytosis — This article is about aspects of spherocytosis specific to the hereditary form[translate.academic.ru] […] dictionary Hereditary pyropoikilocytosis — (HPP) is an autosomal recessive form of hemolytic anemia characterized by an abnormal sensitivity of red blood cells to heat and erythrocyte[translate.academic.ru]

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