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32 Possible Causes for Congenital Nonspherocytic Hemolytic Anemia, Erythrocytes Decreased, Favism

  • Autoimmune Hemolytic Anemia

    Mechanisms of actions include suppression of autoantibody production, reduction in autoantibody affinity, and decreased destruction of erythrocytes by splenic macrophages,[] In patients with Evans syndrome, the mechanism of destruction of erythrocytes is thought to be similar to AIHA.[] Premature destruction of erythrocytes occurs intravascularly or extravascularly. The etiologies of hemolysis often are categorized as acquired or hereditary.[]

  • Glycogen Storage Disease Type 1

    Phk activity in erythrocytes was markedly decreased (12% residual activity) while the parents' erythrocyte Phk activities were in the heterozygote range (mother: 56%; father[] Chronic hepatitis Albuminuria Distal renal tubular acidosis Hepatocellular adenoma Hypocitraturia Cataract Hyperreflexia Gait disturbance Full cheeks Carcinoma Elevated erythrocyte[] […] hypoplastic anemia Hyperkalemia Inflammation of the large intestine Intestinal obstruction Episodic fever Amyloidosis Antinuclear antibody positivity Acute hepatic failure Decreased[]

  • Congenital Hemolytic Anemia

    […] usually excluding hemoglobin abnormalities as well, but rather encompassing defects of glycolysis in the erythrocyte.Glucose-6-phosphate dehydrogenase deficiency (G6PD or favism[] Phosphatidylserine internalization in erythrocytes with the mutant ATP11C was decreased 10-fold compared to that of the control, functionally establishing that ATP11C is a[] […] excluding hemoglobin abdormalities as well, but rather encompassing defects of glycolysis in the erythrocyte. [ 2 ] Glucose-6-phosphate dehydrogenase deficiency (G6PD or favism[]

  • Pyruvate Kinase Deficiency

    […] most prominent of which are those with a congenital or hereditary origin such as, for example, hemoglobinopathies (sickle-cell anemias, Cooley's anemia), enzymopathies (favism[] decreased erythrocyte pyruvate kinase (PK) activity.[] In this later group of "congenital nonspherocytic hemolytic anemias" splenectomy has often been performed but usually does not produce a clinical cure.[]

  • Anemia due to Glutathione Metabolism Disorder

    Anemia, glutathione reductase deficiency Drug-induced enzyme deficiency anemia Erythrocyte enzyme deficiency Erythrocyte uridine diphosphate galactose-4-epimerase deficiency Favism[] Addition of copper to normal erythrocytes led to increased autohemolysis, thermolability of hemoglobin, increased sensitivity to acetylphenylhydrazine, decreased erythrocyte[] D58.9 ICD-10-CM Diagnosis Code D58.9 Hereditary hemolytic anemia, unspecified 2016 2017 2018 2019 Billable/Specific Code nonspherocytic congenital or hereditary NEC D55.8[]

  • Acquired Toxic Hemolytic Anemia

    Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same community[] Premature destruction of red cells occurs through two primary mechanisms: (1) decreased erythrocyte deformability that leads to red-cell sequestration and extravascular haemolysis[] Congenital Nonspherocytic Hemolytic Anemia includes any of a group of inherited anemias characterized by shortened red cell survival, lack of spherocytosis, and normal osmotic[]

  • Congenital Heinz Body Hemolytic Anemia

    G6PD Deficiency Favism Association, What is G6PD Deficiency? Available online at September 2008. Wintrobe's Clinical Hematology. 12th ed.[] erythrocyte life span Double heterozygous sickling disorder Heinz bodies Hematopoietic maturation arrest Hemoglobin A1c above reference range Hemoglobin C disease Hemoglobin[] nonspherocytic hemolytic anemia * (n) 先天性貧血 P614 ** せんてんせいひんけつ PubMed, Scholar, Google, WikiPedia congenital anemia * (n*) 先天性溶血性貧血 *** せんてんせいようけつせいひんけつ シソーラス PubMed, Scholar[]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    Favism Favism has been known since antiquity. Everyone with Favism is G6PD Deficient.[] If t he fluidity of the cell interior or the surplus of cell surface is reduced, the “conformation instability” of the erythrocyte will decrease.[] .: Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: A new variant (type Nordhorn). II.[]

  • Hemolytic Anemia due to a Disorder of Glycolytic Enzymes

    Defective PK catalysis in affected erythrocytes generally results in elevated concentrations of 2,3-diphosphoglycerate (2,3-DPG) and decreased ATP levels relative to cells[] D55 Anemia due to enzyme disorders D55.0 Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency Inclusion term(s): Favism G6PD deficiency anemia D55.1 Anemia due[] Summary Epidemiology PK deficiency is the most frequent cause of congenital nonspherocytic hemolytic anemia with a prevalence estimated at 1/20,000 in the general white population[]

  • Hemolytic Anemia due to Deficient Glutathione Synthesis

    Aside from favism and drug-induction of hemolytic anemia, infection is the most common cause of hemolysis in G6PDH deficient individuals.[] The mild form of glutathione synthetase deficiency (OMIM 231900) is associated with decreased erythrocyte glutathione levels and well-compensated hemolytic disease.[] The anemia that results is a nonspherocytic hemolytic anemia. See also congenital nonspherocytic hemolytic anemia, favism.[]

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