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68 Possible Causes for Anemia, Congenital Nonspherocytic Hemolytic Anemia, Erythrocytes Decreased

  • Hereditary Spherocytosis

    To date only three siblings with coinheritance of sickle cell anemia (SCA) and hereditary spherocytosis (HS) have been reported.[ncbi.nlm.nih.gov] Defects in these proteins lead to a loss in RBC membrane cohesion and membrane surface area, resulting in erythrocyte sphering, decreased deformability and premature destruction[orpha.net] Hereditary spherocytosis (HS) and pyruvate kinase (PK) deficiency are the most common causes of congenital hemolytic anemia.[ncbi.nlm.nih.gov]

  • Autoimmune Hemolytic Anemia

    Autoimmune haemolytic anaemia Autoimmune hemolytic anemia NOS (disorder) Autoimmune hemolytic anemia ANEMIA, AUTOIMMUNE HEMOLYTIC AIHA AHA edit English autoimmune hemolytic[wikidata.org] Mechanisms of actions include suppression of autoantibody production, reduction in autoantibody affinity, and decreased destruction of erythrocytes by splenic macrophages,[doi.org] The National Cancer Institute considers "immunohemolytic anemia", "autoimmune hemolytic anemia", and "immune complex hemolytic anemia" to all be synonyms.[en.wikipedia.org]

  • Congenital Hemolytic Anemia

    Congenital hemolytic anemia refers to hemolytic anemia which is primarily due to congenital disorders.[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] Hemolytic Congenital, Nonspherocytic Anemia: Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there[medconditions.net]

  • Glycogen Storage Disease Type 1

    Other important laboratory values that must be obtained include: CBC and differential (eg, anemia, leukopenia, neutropenia), Gamma glutamyltransferase level, Serum triglyceride[symptoma.com] 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] E70-E88 Metabolic disorders Type 1 Excludes androgen insensitivity syndrome ( E34.5- ) congenital adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias[icd10data.com]

  • Pyruvate Kinase Deficiency

    Pyruvate kinase deficiency is a rare cause of hemolytic anemia and, in its most severe form, requires splenectomy in childhood.[ncbi.nlm.nih.gov] 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]

  • Toxic Hemolytic Anemia

    Most often, with toxic anemia, intravascular hemolysis is observed. Hemolytic anemia can also occur with infectious diseases.[m.iliveok.com] […] and the inability of bone marrow to compensate for the decreased life span.[diagnose-me.com] Research of Toxic Hemolytic Anemia has been linked to Anemia, Anemia, Hemolytic, Poisoning, Pregnancy Complications, Hematologic, Hemolysis (disorder).[novusbio.com]

  • Congenital Dyserythropoietic Anemia

    anemia resulting in cardiac failure and relatively mild dyserythropoietic features on bone marrow aspiration in contrast to severity of anemia.[ncbi.nlm.nih.gov] We also found that erythrocyte anion exchanger 1 protein is decreased in CDA-II homozygotes and obligate carriers alike.[ncbi.nlm.nih.gov] , type I Congenital dyserythropoietic anemia, type II Congenital dyserythropoietic anemia, type III Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism[icd9data.com]

  • Acquired Toxic Hemolytic Anemia

    Rarely, aplastic anemia is due to an inherited (genetic) disorder such as Fanconi anemia.[labtestsonline.org] 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]

  • Traumatic Hemolytic Anemia

    She was postmenopausal with no previous history of anemia, bleeding, or jaundice. Family history of anemia was negative.[bloodjournal.org] […] and the inability of bone marrow to compensate for the decreased life span.[diagnose-me.com] Premature destruction of erythrocytes occurs intravascularly or extravascularly. The etiologies of hemolysis often are categorized as acquired or hereditary.[aafp.org]

  • Congenital Aplastic Anemia

    A seven-year-old girl with Fanconi's anemia-like congenital aplastic anemia and concurrent asplenia without the congenital heart defects or the abdominal heterotaxia is reported[ncbi.nlm.nih.gov] Discussion Aplastic anemia are disorders where there is inadequate production of erythrocytes, granulocytes and platelets caused by decreased bone marrow production leading[pediatriceducation.org] 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]

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