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113 Possible Causes for Arrhythmias Detected Prenatally, Osmotic Fragility Increased

  • Asplenia Syndrome

    Electrocardiogram (ECG): This is useful in the detection of arrhythmias and other abnormalities in cardiac function Echocardiogram: This is a non-invasive imaging technique[symptoma.com] Prenatal ultrasound: It is possible to diagnose AS before birth, as ultrasound can be used to identify cardiac abnormalities and asplenia.[symptoma.com]

  • 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: Arrhythmias Detected Prenatally
  • 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: Arrhythmias Detected Prenatally
  • Fetal Erythroblastosis

    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] […] due to anti-M shows two features that resemble ABO hemolytic disease rather than Rh hemolytic disease: First, the DAT is only weakly positive or negative and second, the osmotic[doi.org]

    Missing: Arrhythmias Detected Prenatally
  • 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: Arrhythmias Detected Prenatally
  • 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: Arrhythmias Detected Prenatally
  • 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: Arrhythmias Detected Prenatally
  • 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: Arrhythmias Detected Prenatally
  • Malaria

    Congenital malaria is usually defined as the detection of asexual forms of Plasmodium spp. in a blood sample of a neonate during perinatal age if there is no possibility of postpartum infection by a mosquito bite. The incidence of congenital malaria is highly variable and seems related to several factors, such as[…][ncbi.nlm.nih.gov]

    Missing: Arrhythmias Detected Prenatally
  • 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: Arrhythmias Detected Prenatally

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