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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[] HS is characterized by the strong family history of anemia, jaundice, splenomegaly and cholelithiasis.[] Frequently there is a family history of anemia, jaundice, cholelithiasis, or splenectomy.[]

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

  • 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.[] A family history of congenital hemolytic anemia or anemia of childhood is typically present.[] congenital nonspherocytic hemolytic anemia that has material basis in homozygous or compound heterozygous mutation in the PKLR gene on chromosome 1q22 pyruvate kinase deficiency[]

  • 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[] […] occasionally Hodgkin Collagen-vascular (autoimmune) diseases, such as systemic lupus erythematosus Risk Factors that may increase your risk of developing autoimmune hemolytic anemia[] 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[]

  • 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[] […] your family medical history.[] […] and your family medical history.[]

  • Congenital Dyserythropoietic Anemia

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

  • Hereditary Sideroblastic Anemia

    ; increase in iron store will need less transferrin, low TIBC).[] 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[] Family history of sideroblastic anaemia [3] There are two forms of sideroblastic anemia: congenital sideroblastic anemia and acquired sideroblastic anemia. [2] Hereditary[]

  • Waters-West Syndrome

    Increased metabolic requirements, neoplasia. PATHOLOGY: Microcytic, hypochromic anemia. Low serum iron. Bone-Marrow will show absence of iron.[] MalaCards based summary : Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities, is also known as hemolytic anemia lethal congenital nonspherocytic[] One should inquire about previous pregnancies and a family history of adverse pregnancy outcomes. Increased HbA2 would suggest a beta-thalassemia.[]

  • 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[] ]) and can be evaluated in the context of family history and ethnicity.[] About […] Red Blood Cell Enzyme Deficiencies These conditions are sometimes called congenital nonspherocytic anemias.[]

  • Hexokinase Deficiency

    Ferritin, iron, and transferrin saturation are increased. Bone marrow shows hypercellularity with increased iron stores, increased sideroblasts, and ring sideroblasts.[] The findings were entirely different from those of subsequently reported cases with congenital, nonspherocytic hemolytic anemia associated only with a specific deficiency[] NSHA is caused by an inherited gene mutation, making a family history an increased risk of having the disease.[]