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58 Possible Causes for Congenital Nonspherocytic Hemolytic Anemia, Erythrocytes Decreased, Pediatric Disorder

  • 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] The 2003 Healthcare Cost and Utilization Project (HCUP) Kids’ Inpatient Database (KID), a robust and widely used measure of pediatric disorders, has estimated that the number[touchoncology.com] Hans-Christoph Rossbach, THE RULE OF FOUR: A SYSTEMATIC APPROACH TO DIAGNOSIS OF COMMON PEDIATRIC HEMATOLOGIC AND ONCOLOGIC DISORDERS, Fetal and Pediatric Pathology, 24, 6[doi.org]

  • 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] Hemolytic anemia Hereditary elliptocytosis Hereditary pyropoikilocytosis Red cell membrane disorder Pediatrics, Perinatology, and Child Health Hematology Oncology Cite this[scholars.northwestern.edu] 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]

  • 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] Nelson Textbook of Pediatrics. 16th ed. Philadelphia: Saunders; 2000. p. 405. 6. Bickel H, Manz F.[journalofpediatriccriticalcare.com] Chronic hepatitis Albuminuria Distal renal tubular acidosis Hepatocellular adenoma Hypocitraturia Cataract Hyperreflexia Gait disturbance Full cheeks Carcinoma Elevated erythrocyte[mendelian.co]

  • Pyruvate Kinase Deficiency

    decreased erythrocyte pyruvate kinase (PK) activity.[ncbi.nlm.nih.gov] Stephen Rogers, Manuel Silva and Allan Doctor, Hematologic Disorders, Studies on Pediatric Disorders, 10.1007/978-1-4939-0679-6_21, (349-369), (2014).[dx.doi.org] In this later group of "congenital nonspherocytic hemolytic anemias" splenectomy has often been performed but usually does not produce a clinical cure.[nejm.org]

  • 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] Hereditary Elliptocytosis and Related Disorders Pediatric Lead Toxicity Pediatric Megaloblastic Anemia Pediatric Myelodysplastic Syndrome Sickle Cell Anemia Transient Erythroblastopenia[emedicine.medscape.com] , type I Congenital dyserythropoietic anemia, type II Congenital dyserythropoietic anemia, type III Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism[icd9data.com]

  • Congenital Hypoplastic Anemia

    The second of these cases provided an unusual opportunity to study human erythrocyte precursor dynamics.[ncbi.nlm.nih.gov] Succinct, targeted coverage of normal childhood growth and development, as well as the diagnosis, management, and prevention of common pediatric diseases and disorders, make[books.google.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]

  • Congenital Aplastic Anemia

    Discussion Aplastic anemia are disorders where there is inadequate production of erythrocytes, granulocytes and platelets caused by decreased bone marrow production leading[pediatriceducation.org] Aplastic Anemia Treatment at Dana-Farber/Boston Children's Children and young adults with aplastic anemia are treated at Dana-Farber/Boston Children's Cancer and Blood Disorders[childrenshospital.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]

  • 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] Exclusive bonus features include Diagnosaurus DDx, 200 pediatrics topics, and medical news feeds.[unboundmedicine.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]

  • 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] Autoimmune hemolytic anemia is a rare disorder in pediatric population and most respond well to steroids regardless of the type of antibody.[ncbi.nlm.nih.gov] Treatment with rituximab in benign and malignant hematologic disorders in children.[link.springer.com]

  • Fetal Erythroblastosis

    Data Cues list assessment data to help you recognize possible pediatric disorders.[books.google.de] The phenotype of severe nonspherocytic hemolytic anemia, jaundice, hepatosplenomegaly, and marked erythroblastosis is more severe than that present in congenital dyserythropoietic[readbyqxmd.com] Pediatr Res. 1997;41:716-21. Mentzer WC, Glader BE. Erythrocyte disorders in infancy. In: Taeusch WH, Ballard RA, Gleason CA, editors., eds.[doi.org]

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