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

  • Hereditary Spherocytosis

    A detailed medical history will help uncover possible risk factors for anemia such as a family history of anemia, certain medications, chronic infection, intestinal disorders[livestrong.com] HS is characterized by the strong family history of anemia, jaundice, splenomegaly and cholelithiasis.[mjdrdypu.org] Frequently there is a family history of anemia, jaundice, cholelithiasis, or splenectomy.[healio.com]

  • 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] He is the second son of a non-consanguineous couple with unremarkable family history; there were no records of anemia, jaundice, gallstones or splenomegaly.[casesjournal.biomedcentral.com] 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]

  • 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] A family history of congenital hemolytic anemia or anemia of childhood is typically present.[clinicaladvisor.com] 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]

  • Autoimmune Hemolytic Anemia

    […] include: Recent viral infections Taking medications that can cause autoimmune hemolytic anemia Cancer Collagen-vascular (autoimmune) disease Family history of hemolytic disease[winchesterhospital.org] […] occasionally Hodgkin Collagen-vascular (autoimmune) diseases, such as systemic lupus erythematosus Risk Factors that may increase your risk of developing autoimmune hemolytic anemia[cancercarewny.com] These include people with diets poor in iron and vitamins, chronic diseases such as kidney disease, diabetes, cancer, inflammatory bowel disease, a family history of inherited[labtestsonline.org]

  • 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] […] your family medical history.[daviddarling.info] […] and your family medical history.[theoncologyinstitute.com]

  • Congenital Dyserythropoietic Anemia

    Iron stores were increased although ring sideroblasts were absent.[ncbi.nlm.nih.gov] , type I Congenital dyserythropoietic anemia, type II Congenital dyserythropoietic anemia, type III Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism[icd9data.com] CASE REPORT The patient was born to nonconsanguineous, healthy parents without a family history of anemia.[journals.lww.com]

  • Hereditary Sideroblastic Anemia

    ; increase in iron store will need less transferrin, low TIBC).[forums.studentdoctor.net] 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] Family history of sideroblastic anaemia [3] There are two forms of sideroblastic anemia: congenital sideroblastic anemia and acquired sideroblastic anemia. [2] Hereditary[explainmedicine.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] One should inquire about previous pregnancies and a family history of adverse pregnancy outcomes. Increased HbA2 would suggest a beta-thalassemia.[emedicine.medscape.com]

  • 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] ]) and can be evaluated in the context of family history and ethnicity.[oncologynurseadvisor.com] About […] Red Blood Cell Enzyme Deficiencies These conditions are sometimes called congenital nonspherocytic anemias.[med-life.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] The findings were entirely different from those of subsequently reported cases with congenital, nonspherocytic hemolytic anemia associated only with a specific deficiency[jamanetwork.com] NSHA is caused by an inherited gene mutation, making a family history an increased risk of having the disease.[diseaseinfosearch.org]