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1,095 Possible Causes for Congenital Hemolytic Anemia, Non-Hemolytic Unconjugated Hyperbilirubinemia

  • Gilbert Syndrome

    Constitutional liver dysfunction Familial non-hemolytic non-obstructive jaundice Icterus intermittens juvenilis Low-grade chronic hyperbilirubinemia Unconjugated benign bilirubinemia[] […] adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4 ) 5-alpha-reductase[] Tagged as: constitutional liver dysfunction, familial benign unconjugated hyperbilirubinaemia, familial non-hemolytic non-obstructive jaundice, Gilbert–Meulengracht syndrome[]

  • Pyruvate Kinase Deficiency

    It constitutes one of the common causes of hereditary non-spherocytic hemolytic anemia.[] HEREDITARY spherocytosis with its associated congenital hemolytic anemia is generally easily recognized and satisfactorily treated with splenectomy.[] Pyruvate kinase deficiency is a rare cause of congenital hemolytic anemia.[]

  • Crigler-Najjar Syndrome Type 1

    Mutations in the UGT1A1 gene cause Crigler-Najjar syndrome (CN), which causes non-hemolytic unconjugated hyperbilirubinemia, and is categorized as CN1 and CN2 according to[] […] adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4 ) 5-alpha-reductase[] Crigler-Najjar (CN) syndrome is a rare autosomal recessive inherited disorder characterized by non-hemolytic, unconjugated hyperbilirubinemia.[]

  • Hereditary Spherocytosis

    […] biconcave disk shape Congenital spherocytic hemolytic anemia Minkowski Chauffard syndrome spherocytic anemia edit English hereditary spherocytosis congenital hemolytic anemia[] Abstract Hereditary spherocytosis (HS) is a disease affecting the red blood cells membrane and belongs to the congenital hemolytic anemias.[] 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[]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Hemoglobinopathy

    BACKGROUND: Hemoglobinopathies are a very heterogeneous group of congenital hemolytic anemia.[] […] persistence of fetal hemoglobin) ("Swiss variety") 282.7 unstable hemoglobin hemolytic 282.7 Elliptocytosis (congenital) (hereditary) 282.1 Hb-C (disease) 282.7 hemoglobin[] 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[]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Erythrocyte Membrane Abnormality

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

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Autoimmune Hemolytic Anemia

    […] from congenital hemolytic anemia.[] 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[] 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[]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Cooley's Anemia

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

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Hemolytic Anemia

    A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.[] Congenital Hemolytic Anemia In congenital hemolytic anemias, the destruction of red blood cells is caused by a defect within the red blood cells themselves.[] Congenital hemolytic anemias are present at birth and may or may not be inherited.[]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • 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[] […] adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4 ) 5-alpha-reductase[] Pyruvate kinase deficiency is the most common glycolytic enzyme deficiency that leads to life-long hemolytic anemia.[]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia

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