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134 Possible Causes for Icterus Gravis Neonatorum, Osmotic Fragility Increased

  • Fetal Erythroblastosis

    […] disease hemolytic newborns , erythroblastosis fetalis , disease hemolytic newborn , disease hemolytic of newborn , diseases hemolytic newborn , icterus gravis neonatorum ,[fpnotebook.com] fragility of the red cells may be greatly increased. [3], [18] As all other cell lines were in normal range with a low reticulocyte count since birth indicating a possible[doi.org] Plasmapheresis was given from 17 weeks of gestation but fetal erythroblastosis still developed 1 week later.[ncbi.nlm.nih.gov]

  • Third Trimester Pregnancy

    The concomitant phenomenon of a third trimester pregnancy with a significant degree of pelvic organ prolapse is extremely rare. We report on a patient with pelvic organ prolapse complicating third trimester pregnancy treated by concomitant cesarean hysterectomy and abdominal sacrocolpopexy. A 30-year-old woman,[…][ncbi.nlm.nih.gov]

    Missing: Icterus Gravis Neonatorum
  • Hereditary Spherocytosis

    fragility: increased; basis for diagnostic testing Diagrams / tables Images hosted on other servers: Scatter diagram of CBC Treatment Splenectomy (prolongs survival of red[pathologyoutlines.com] Blood film showed about 70% spherocytes, reticulocytosis of 6.5%, increased osmotic fragility test and a negative direct antiglobulin test.[ncbi.nlm.nih.gov] The evaluation of her mother revealed spherocytosis with anemia and increased osmotic fragility of RBCs.[indianjnephrol.org]

    Missing: Icterus Gravis Neonatorum
  • Congenital Hemolytic Anemia

    Osmotic fragility of fresh blood was increased, and postsplenectomy blood showed a fraction of extremely fragile cells.[ncbi.nlm.nih.gov] 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[bloodjournal.org] The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.[icd9data.com]

    Missing: Icterus Gravis Neonatorum
  • Chronic Lymphocytic Leukemia

    Chronic lymphocytic leukemia (CLL) is the commonest leukemia in western countries. The disease typically occurs in elderly patients and has a highly variable clinical course. Leukemic transformation is initiated by specific genomic alterations that impair apoptosis of clonal B cells. The diagnosis is established by blood[…][ncbi.nlm.nih.gov]

    Missing: Icterus Gravis Neonatorum
  • Paroxysmal Nocturnal Hemoglobinuria

    Paroxysmal nocturnal hemoglobinuria is a rare clonal hematopoietic stem cell disorder characterized by intravascular hemolysis, hemoglobinuria, and inflammatory thrombotic state. Intravascular hemolysis in paroxysmal nocturnal hemoglobinuria (PNH) can lead to acute and chronic renal injury through hemoglobin-mediated[…][ncbi.nlm.nih.gov]

    Missing: Icterus Gravis Neonatorum
  • Autoimmune Hemolytic Anemia

    Autoimmune hemolytic anemia (AIHA) is a relatively uncommon disorder caused by autoantibodies directed against self red blood cells. It can be idiopathic or secondary, and classified as warm, cold (cold hemagglutinin disease (CAD) and paroxysmal cold hemoglobinuria) or mixed, according to the thermal range of the[…][ncbi.nlm.nih.gov]

    Missing: Icterus Gravis Neonatorum
  • Malaria

    BACKGROUND: Plasmodium knowlesi is increasingly recognized as a cause of human malaria in Southeast Asia but there are no detailed prospective clinical studies of naturally acquired infections. METHODS: In a systematic study of the presentation and course of patients with acute P. knowlesi infection, clinical and[…][ncbi.nlm.nih.gov]

    Missing: Icterus Gravis Neonatorum
  • Glycogen Storage Disease Type 1

    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 (G6P) to glucose. GSD1 is associated with severe hyperlipidaemia and hepatic steatosis. The underlying mechanisms responsible for these[…][ncbi.nlm.nih.gov]

    Missing: Icterus Gravis Neonatorum
  • Hereditary Elliptocytosis

    MCHC more than 36% C. increased osmotic fragility D. all of the above D. all of the above spherocytes on the peripheral smear MCHC more than 36% increased osmotic fragility[quizlet.com] fragility test Osmotic fragility is increased because of red cell membrane instability. [17] Autohemolysis test, the hypertonic cryohemolysis test, and the acidified glycerol[explainmedicine.com] Diagnosis requires demonstration of increased RBC osmotic fragility and a negative direct antiglobulin test.[msdmanuals.com]

    Missing: Icterus Gravis Neonatorum

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