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49 Possible Causes for Congenital Nonspherocytic Hemolytic Anemia, Erythrocytes Decreased, Family History of Anemia

  • Hereditary Spherocytosis

    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] HS is characterized by the strong family history of anemia, jaundice, splenomegaly and cholelithiasis.[mjdrdypu.org] Stability studies with blood from HS patients showed a significant decrease in hyperchromic erythrocytes after 6 h storage.[ncbi.nlm.nih.gov]

  • Congenital Hemolytic Anemia

    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] This group is sometimes called congenital nonspherocytic (hemolytic) anemia, which is a term for a congenital hemolytic anemia without spherocytosis, and usually excluding[en.wikipedia.org] He is the second son of a non-consanguineous couple with unremarkable family history; there were no records of anemia, jaundice, gallstones or splenomegaly.[casesjournal.biomedcentral.com]

  • 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]

  • Pyruvate Kinase Deficiency

    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] A family history of congenital hemolytic anemia or anemia of childhood is typically present.[clinicaladvisor.com]

  • 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] […] include: Recent viral infections Taking medications that can cause autoimmune hemolytic anemia Cancer Collagen-vascular (autoimmune) disease Family history of hemolytic disease[winchesterhospital.org] […] occasionally Hodgkin Collagen-vascular (autoimmune) diseases, such as systemic lupus erythematosus Risk Factors that may increase your risk of developing autoimmune hemolytic anemia[cancercarewny.com]

  • Congenital Dyserythropoietic Anemia

    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] CASE REPORT The patient was born to nonconsanguineous, healthy parents without a family history of anemia.[journals.lww.com]

  • Traumatic Hemolytic Anemia

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

  • Hereditary Sideroblastic Anemia

    […] and gama-interferon inhibit red cell production Shortened erythrocyte survival Autoimmune diseases may also cause antibody-mediated destruction CBC: Mild anemia (Hgb 9-11[quizlet.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] Family history of sideroblastic anaemia [3] There are two forms of sideroblastic anemia: congenital sideroblastic anemia and acquired sideroblastic anemia. [2] Hereditary[explainmedicine.com]

  • Toxic Hemolytic Anemia

    […] and the inability of bone marrow to compensate for the decreased life span.[diagnose-me.com] Some of the important features in medical history cover questions about family history, previous personal history of anemia or other chronic conditions, medications, color[emedicinehealth.com] history should be positive, DAT positive in AIHA, negative in hereditary spherocytosis.[pedclerk.bsd.uchicago.edu]

  • Anemia due to Glutathione Metabolism Disorder

    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] , and its diagnosis should be considered in children with a family history of jaundice, anemia, splenomegaly, or cholelithiasis, especially in those of Mediterranean or African[aafp.org]

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