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

  • Hereditary Spherocytosis

    To date only three siblings with coinheritance of sickle cell anemia (SCA) and hereditary spherocytosis (HS) have been reported.[ncbi.nlm.nih.gov] Hereditary spherocytosis (HS) and pyruvate kinase (PK) deficiency are the most common causes of congenital hemolytic anemia.[ncbi.nlm.nih.gov] Describing 6 typical cases, we demonstrate that occasional normal percentages of hyperchromic red blood cells occurring during phases of anemia and/or iron deficiency are[ncbi.nlm.nih.gov]

  • Autoimmune Hemolytic Anemia

    Autoimmune haemolytic anaemia Autoimmune hemolytic anemia NOS (disorder) Autoimmune hemolytic anemia ANEMIA, AUTOIMMUNE HEMOLYTIC AIHA AHA edit English autoimmune hemolytic[wikidata.org] The National Cancer Institute considers "immunohemolytic anemia", "autoimmune hemolytic anemia", and "immune complex hemolytic anemia" to all be synonyms.[en.wikipedia.org] Cold antibody hemolytic anemia is common among the elderly, while warm antibody hemolytic anemia affects all age groups.[symptoma.com]

  • Congenital Hemolytic Anemia

    Congenital hemolytic anemia refers to hemolytic anemia which is primarily due to congenital disorders.[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

    Pyruvate kinase deficiency is a rare cause of hemolytic anemia and, in its most severe form, requires splenectomy in childhood.[ncbi.nlm.nih.gov] 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]

  • Acquired Toxic Hemolytic Anemia

    Rarely, aplastic anemia is due to an inherited (genetic) disorder such as Fanconi anemia.[labtestsonline.org] 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] Living with hemolytic anemia The course of hemolytic anemia depends on the cause and the severity of the anemia. Mild hemolytic anemia may need no treatment at all.[daviddarling.info]

  • Congenital Heinz Body Hemolytic Anemia

    Abstract The mechanisms of hemoglobin precipitation into Heinz bodies and hemolytic anemia that characterize congenital Heinz body hemolytic anemia (CHBHA) were studied in[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] CHBHA stands for "Congenital Heinz Body Hemolytic Anemia" How to abbreviate Congenital Heinz Body Hemolytic Anemia?[allacronyms.com]

  • 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] Homepage Rare diseases Search Search for a rare disease Lethal hemolytic anemia-genital anomalies syndrome Disease definition Waters-West syndrome is characterized by the[orpha.net]

  • 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] It is likely, although not certain, that in this patient nonspherocytic hemolytic anemia resulted from hexokinase deficiency.[ncbi.nlm.nih.gov] The findings were entirely different from those of subsequently reported cases with congenital, nonspherocytic hemolytic anemia associated only with a specific deficiency[jamanetwork.com]

  • 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] Acquired hemolytic anemia can be divided into immune and non-immune mediated forms of hemolytic anemia.[en.wikipedia.org] 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]

  • Red Blood Cell Disorder

    […] education to ultimately find a cure Sickle Cell Disease Association of America National Lung, Heart and Blood Institute Sickle cell disease Other blood diseases Cooley's Anemia[chla.org] Ferritin: soluble iron binding storage protein also helps to keep iron in its non toxic form. Its synthesized by the bone marrow macrophages and hepatocytes.[slideplayer.com] 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]

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