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173 Possible Causes for Congenital Nonspherocytic Hemolytic Anemia

  • Hereditary Spherocytosis

    Hereditary spherocytosis is a condition that affects red blood cells. People with this condition typically experience a shortage of red blood cells ( anemia ), yellowing of the eyes and skin (jaundice), and an enlarged spleen (splenomegaly). Most newborns with hereditary spherocytosis have severe anemia, although it[…][ghr.nlm.nih.gov]

  • Autoimmune Hemolytic Anemia

    Treatment of autoimmune hemolytic anemias Haematologica October 2014 99: 1547-1554; doi: 10.3324/haematol.2014.114561 Abstract Autoimmune hemolytic anemia (AIHA) is a relatively uncommon disorder caused by autoantibodies directed against self red blood cells. It can be idiopathic or secondary, and classified as warm,[…][doi.org]

  • Glycogen Storage Disease Type 1

    Glycogen storage disease type XI is a form of glycogen storage disease. It is also known for Guido Fanconi and Horst Bickel, who first described it in 1949. It is associated with GLUT2, a glucose transport protein which, when functioning normally, allows glucose to exit several tissues, including the liver, nephrons, and[…][en.wikipedia.org]

  • Congenital Hemolytic Anemia

    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] 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] Microangiopathic hemolytic anemia Classification and external resources ICD 10 D59.4 ICD 9 … Wikipedia nonspherocytic hemolytic anemia — see congenital nonspherocytic hemolytic[en.academic.ru]

  • Pyruvate Kinase Deficiency

    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 nonspherocytic hemolytic anemia that has material basis in homozygous or compound heterozygous mutation in the PKLR gene on chromosome 1q22 pyruvate kinase deficiency[wikidata.org] The sisters were diagnosed at birth with profound jaundice and congenital nonspherocytic hemolytic anemia.[ncbi.nlm.nih.gov]

  • Hemolytic Anemia due to a Disorder of Glycolytic Enzymes

    Summary Epidemiology PK deficiency is the most frequent cause of congenital nonspherocytic hemolytic anemia with a prevalence estimated at 1/20,000 in the general white population[orpha.net] anemia and congenital hemolytic anemia.[malacards.org] , as an aid in searching Hereditary nonspherocytic hemolytic anemia Congenital hemolytic anemia Adenlyate kinase deficiency AK AK1 ALDOA Aldolase A deficiency ALDOA deficiency[mayomedicallaboratories.com]

  • Acquired Hemolytic Anemia

    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] congenital hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency, acquired hemolytic anemia and vitamin B12 deficiency induced megaloblastic anemia..[ncbi.nlm.nih.gov] 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]

  • Lethal Hemolytic Anemia-Genital Anomalies Syndrome

    MalaCards based summary : Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities, is also known as hemolytic anemia lethal congenital nonspherocytic[malacards.org] Anemia, Hemolytic , Congenital Nonspherocytic Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there[ncbi.nlm.nih.gov] Anemia, Lethal Congenital Nonspherocytic, With Genital Andother Abnormalities Hydrocephalus, Sprengel Anomaly, And Costovertebral Dysplasia Lethal Faciocardiomelic Dysplasia[familydiagnosis.com]

  • Red Blood Cell Disorder

    Summary Epidemiology PK deficiency is the most frequent cause of congenital nonspherocytic hemolytic anemia with a prevalence estimated at 1/20,000 in the general white population[orpha.net] , as in patients with congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase or pyruvate kinase deficiency.[mayomedicallaboratories.com] Interfering factors: -Recent transfusion -Oral contraceptives -H2 blockers Infrequently, other hemolytic disorders may also be associated with positive osmotic fragility results[mayomedicallaboratories.com]

  • Hexokinase Deficiency

    The findings were entirely different from those of subsequently reported cases with congenital, nonspherocytic hemolytic anemia associated only with a specific deficiency[jamanetwork.com] […] recessive inheritance ; Cholecystitis ; Cholelithiasis ; Congenital onset ; Hyperbilirubinemia ; Jaundice ; Nonspherocytic hemolytic anemia ; Normochromic anemia ; Normocytic[mousephenotype.org] Congenital nonspherocytic hemolytic anemia -Some rare variants of G6PD deficiency are so severe that hemolysis is constant.[web.archive.org]

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