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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,[doi.org] In patients with Evans syndrome, the mechanism of destruction of erythrocytes is thought to be similar to AIHA.[cancertherapyadvisor.com] Premature destruction of erythrocytes occurs intravascularly or extravascularly. The etiologies of hemolysis often are categorized as acquired or hereditary.[aafp.org]

  • 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[academic.oup.com] Chronic hepatitis Albuminuria Distal renal tubular acidosis Hepatocellular adenoma Hypocitraturia Cataract Hyperreflexia Gait disturbance Full cheeks Carcinoma Elevated erythrocyte[mendelian.co] […] hypoplastic anemia Hyperkalemia Inflammation of the large intestine Intestinal obstruction Episodic fever Amyloidosis Antinuclear antibody positivity Acute hepatic failure Decreased[mendelian.co]

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

  • 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[fcarreras.org] decreased erythrocyte pyruvate kinase (PK) activity.[ncbi.nlm.nih.gov] In this later group of "congenital nonspherocytic hemolytic anemias" splenectomy has often been performed but usually does not produce a clinical cure.[nejm.org]

  • 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[icd9data.com] Addition of copper to normal erythrocytes led to increased autohemolysis, thermolability of hemoglobin, increased sensitivity to acetylphenylhydrazine, decreased erythrocyte[annals.org] 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[icd10data.com]

  • 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[arupconsult.com] Premature destruction of red cells occurs through two primary mechanisms: (1) decreased erythrocyte deformability that leads to red-cell sequestration and extravascular haemolysis[oxfordmedicine.com] Congenital Nonspherocytic Hemolytic Anemia includes any of a group of inherited anemias characterized by shortened red cell survival, lack of spherocytosis, and normal osmotic[diagnose-me.com]

  • Congenital Heinz Body Hemolytic Anemia

    G6PD Deficiency Favism Association, What is G6PD Deficiency? Available online at September 2008. Wintrobe's Clinical Hematology. 12th ed.[labtestsonline.it] erythrocyte life span Double heterozygous sickling disorder Heinz bodies Hematopoietic maturation arrest Hemoglobin A1c above reference range Hemoglobin C disease Hemoglobin[icd9data.com] 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[lsd-project.jp]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    Favism Favism has been known since antiquity. Everyone with Favism is G6PD Deficient.[g6pddeficiency.org] If t he fluidity of the cell interior or the surplus of cell surface is reduced, the “conformation instability” of the erythrocyte will decrease.[content.iospress.com] .: Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: A new variant (type Nordhorn). II.[link.springer.com]

  • 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[ommbid.mhmedical.com] 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[icd10coded.com] 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[orpha.net]

  • 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.[themedicalbiochemistrypage.org] The mild form of glutathione synthetase deficiency (OMIM 231900) is associated with decreased erythrocyte glutathione levels and well-compensated hemolytic disease.[ommbid.mhmedical.com] The anemia that results is a nonspherocytic hemolytic anemia. See also congenital nonspherocytic hemolytic anemia, favism.[medical-dictionary.thefreedictionary.com]

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