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321 Possible Causes for Bone Marrow with Erythrophagocytosis, Bone Marrow with Increased Iron Stores, Congenital Nonspherocytic Hemolytic Anemia

  • Autoimmune Hemolytic Anemia

    Immune checkpoint inhibitors (ICIs) have demonstrated efficacy against various types of cancers. In addition to immune-related adverse events (irAEs) induced by ICIs, exacerbation of baseline autoimmune disease has been occasionally reported. This is the first report of autoimmune hemolytic anemia (AIHA) exacerbated[…][ncbi.nlm.nih.gov]

  • 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]

  • Hereditary Spherocytosis

    Da Wikimedia Commons, l'archivio di file multimediali liberi Jump to navigation Jump to search sferocitosi ereditaria disordine emolitico di carattere ereditario, autosomico dominante[ Carica un file multimediale Wikipedia Istanza di malattia Sottoclasse di congenital hemolytic anemia, Sferocitosi Controllo di autorità Q541244[…][commons.wikimedia.org]

    Missing: Bone Marrow with Erythrophagocytosis
  • 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]

    Missing: Bone Marrow with Erythrophagocytosis
  • Acquired Toxic 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 is a general term for hemolytic anemia that is present from birth and in which the lifespan of red blood cells is diminished, such as occurs in[diagnose-me.com]

    Missing: Bone Marrow with Erythrophagocytosis
  • Waters-West Syndrome

    Increased metabolic requirements, neoplasia. PATHOLOGY: Microcytic, hypochromic anemia. Low serum iron. Bone-Marrow will show absence of iron.[kumc.edu] 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]

    Missing: Bone Marrow with Erythrophagocytosis
  • Congenital Heinz Body Hemolytic Anemia

    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] About […] Red Blood Cell Enzyme Deficiencies These conditions are sometimes called congenital nonspherocytic anemias.[med-life.net] Usually the anemia is episodic, but some of the unusual variants of G-6-PD may cause nonspherocytic congenital hemolytic disease (see below).[g6pd.org]

    Missing: Bone Marrow with Erythrophagocytosis
  • Anemia of Chronic Disease

    Bone marrow iron stores are usually increased. Ferritin (an acute phase reactant) may be elevated in inflammation.[med-ed.virginia.edu] […] and bone marrow invasion by tumour cells and pathogens.[ncbi.nlm.nih.gov] Hepcidin is a key that locks up iron in the bone marrow and prevents it’s release to transferrin. That’s why, ferritin is increased. (Stores are there, but unavailable!)[medicowesome.com]

    Missing: Congenital Nonspherocytic Hemolytic Anemia
  • Hexokinase Deficiency

    Ferritin, iron, and transferrin saturation are increased. Bone marrow shows hypercellularity with increased iron stores, increased sideroblasts, and ring sideroblasts.[web.archive.org] 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]

    Missing: Bone Marrow with Erythrophagocytosis
  • Acquired Hemolytic Anemia

    Assuming the bone marrow is normal and there are sufficient erythropoeitin and iron stores, acute anemia (ie. hemolysis or blood loss) should increase the retic % to 4-6%[errolozdalga.com] 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]

    Missing: Bone Marrow with Erythrophagocytosis