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736 Possible Causes for Congenital Hemolytic Anemia

  • Hereditary Spherocytosis

    […] biconcave disk shape Congenital spherocytic hemolytic anemia Minkowski Chauffard syndrome spherocytic anemia edit English hereditary spherocytosis congenital hemolytic anemia[wikidata.org] Abstract Hereditary spherocytosis (HS) is a disease affecting the red blood cells membrane and belongs to the congenital hemolytic anemias.[ncbi.nlm.nih.gov] From Wikidata Jump to navigation Jump to search congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal[wikidata.org]

  • Hemoglobinopathy

    BACKGROUND: Hemoglobinopathies are a very heterogeneous group of congenital hemolytic anemia.[ncbi.nlm.nih.gov] […] persistence of fetal hemoglobin) ("Swiss variety") 282.7 unstable hemoglobin hemolytic 282.7 Elliptocytosis (congenital) (hereditary) 282.1 Hb-C (disease) 282.7 hemoglobin[icd9data.com] Anomaly hemoglobin (see also Disease, hemoglobin) 282.7 Anemia 285.9 Heinz-body, congenital 282.7 Disease, diseased - see also Syndrome hemoglobin (Hb) 282.7 HPFH (hereditary[icd9data.com]

  • Erythrocyte Membrane Abnormality

    .: Congenital hemolytic anemia with high-sodium, low-potassium red cells. New Engl. J. Med. 280 , 909 (1969) PubMed Google Scholar 18.[link.springer.com] […] support Publication types Research Support, N.I.H., Extramural Review MeSH terms Anemia, Hemolytic, Congenital/blood* Anemia, Hemolytic, Congenital/complications Anemia,[ncbi.nlm.nih.gov] […] ulcerative colitis Hemolytic anemia, hereditary Hemolytic anemia, lymphoproliferative disease Hemolytic anemia, with ulcerative colitis Hereditary hemolytic anemia Clinical[icd10data.com]

  • Autoimmune Hemolytic Anemia

    […] from congenital hemolytic anemia.[en.wikipedia.org] Causes of and Risk Factors for Hemolytic Anemia There are two major types of hemolytic anemia: Congenital hemolytic anemia is a condition in which red blood cells die off[everydayhealth.com] Enzyme Deficiency Congenital Hemolytic Anemias: G6PD deficiency, pyruvate kinase deficiency, and others AIHA could be confused with a hemolytic crisis in patients with G-6[oncologynurseadvisor.com]

  • Cooley's Anemia

    , Congenital Anemia, Hemolytic Hemoglobinopathies Genetic Diseases, Inborn Iron Metabolism Disorders Lung Diseases Respiratory Tract Diseases Sildenafil Citrate Decitabine[clinicaltrials.gov] Iron Overload Hematologic Diseases beta-Thalassemia Hypertension, Pulmonary Bone Diseases, Metabolic Bone Diseases Musculoskeletal Diseases Metabolic Diseases Anemia, Hemolytic[clinicaltrials.gov] Publications: Keywords provided by New England Research Institutes: chelator iron transfusion anemia thalassemia Additional relevant MeSH terms: Anemia Osteoporosis Thalassemia[clinicaltrials.gov]

  • Glycogen Storage Disease Type 1

    Pyrimidine 5' nucleotidase deficiency presents with congenital hemolytic anemia because the residual nucleotides in young red cells (reticulocytes) cannot be metabolized and[cancertherapyadvisor.com] […] adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4 ) 5-alpha-reductase[icd10data.com] Pyruvate kinase deficiency is the most common glycolytic enzyme deficiency that leads to life-long hemolytic anemia.[cancertherapyadvisor.com]

  • Pyruvate Kinase Deficiency

    HEREDITARY spherocytosis with its associated congenital hemolytic anemia is generally easily recognized and satisfactorily treated with splenectomy.[nejm.org] Abstract Pyruvate kinase deficiency is a rare cause of congenital hemolytic anemia.[ncbi.nlm.nih.gov] Taking into account that pyruvate kinase deficiency is the second most common cause of nonspherocytic congenital hemolytic anemia, detection of deficient cases by genetic[ncbi.nlm.nih.gov]

  • Hemoglobin SC Disease

    Abstract We retrospectively examined the medical and autopsy records of seven previously unpublished cases of fatal pneumococcal septicemia in children with hemoglobin SC disease. The earliest death occurred in a 1-year-old child who had congenital heart disease with cyanosis; the other children were aged 3 1/2 to[…][ncbi.nlm.nih.gov]

  • Sickle Cell Disease

    PURPOSE: Retinal ischemia is a pathophysiologic feature of sickle cell retinopathy. Inner retinal thinning of retina temporal to the fovea has been reported on spectral-domain optical coherence tomography (SD-OCT) even though clinical examination is normal and fluorescein angiography (FA) does not show any capillary[…][ncbi.nlm.nih.gov]

  • Congenital Hemolytic Anemia

    Congenital hemolytic anemia refers to hemolytic anemia which is primarily due to congenital disorders.[en.wikipedia.org] Abstract We characterized the pathologic changes in 50 spleens from patients with autoimmune hemolytic anemia and in 13 spleens from patients with congenital hemolytic anemia[ncbi.nlm.nih.gov] , Hemolytic, Congenital/pathology Anemia, Hemolytic, Congenital/surgery* Anemia, Sickle Cell/pathology Anemia, Sickle Cell/surgery* Ankyrins/deficiency* Bilirubin/blood Child[ncbi.nlm.nih.gov]

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