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404 Possible Causes for Bone Marrow with Increased Iron Stores, Cataracts Usually Congenital

  • Hemochromatosis

    […] levels usually normal or low) II.[] cataracts) Neuroferritinopathy (autosomal dominant genetic disorder affecting basal ganglai; clinical onset in adulthood, iron and ferritin deposits in the brain, ferritin[] H-ferritin mutation Hyperferritinemia without iron overload (autosomal dominant genetic disorder causing high ferritin levels without iron overload; associated with bilateral congenital[]

  • Hypomyelinating Leukodystrophy Type 5

    The infant may also need to be treated for the inherited disorder that is causing the cataracts. Removing a congenital cataract is usually a safe, effective procedure.[] Hypomyelination and congenital cataract (HCC) is usually characterized by bilateral congenital cataracts and normal psychomotor development in the first year of life, followed[] […] typical peripheral nervous system involvement hypomyelination with congenital cataract 4H syndrome : hypomyelination, hypogonadotropic hypogonadism, and hypodontia Cockayne[]

    Missing: Bone Marrow with Increased Iron Stores
  • Rheumatoid Arthritis

    A 65-year-old female had been treated rheumatoid arthritis (RA), interstitial pneumonia (IP) and nephrotic syndrome with prednisolone and cyclosporine. She was emergently admitted to our hospital due to the worsening exertional dyspnea and severe hypoxemia. Chest computed tomography (CT) showed new diffuse[…][]

    Missing: Cataracts Usually Congenital
  • Inflammatory Bowel Disease

    Abstract Elderly-onset inflammatory bowel disease (IBD) will be seen more frequently with the ageing of the population and the increasing incidence of IBD. However, knowledge regarding the best approach to IBD in this population is scarce. Furthermore, differential diagnosis in elderly patients with diarrhoea, rectal[…][]

    Missing: Cataracts Usually Congenital
  • Hereditary Spherocytosis

    The term blueberry muffin rash is used to describe the clinical presentation of dermal extramedullary hematopoiesis. The common culprits of this rash include a TORCH (toxoplasmosis, other agents, rubella, cytomegalovirus, herpes) infection or hematologic dyscrasia. Association of this rash with hereditary[…][]

    Missing: Cataracts Usually Congenital
  • Pernicious Anemia

    Autoimmun Rev. 2014 Apr-May;13(4-5):565-8. doi: 10.1016/j.autrev.2014.01.042. Epub 2014 Jan 11. Author information 1 Laboratory of Clinical Pathology, San Antonio Hospital, via Morgagni 18, 33028 Tolmezzo, UD, Italy. Electronic address: 2 Laboratory of Clinical Pathology, Civic Hospital, via[…][]

    Missing: Cataracts Usually Congenital
  • Anemia of Infection

    Abstract A major factor in the anemia of infection, inflammation, and malignancy is a relative failure of the bone marrow to increase erythropoiesis in response to a shortened red cell survival. The possible causes for this diminished marrow response are: (a) a reduced production of erythropoietin, or, (b) impaired[…][]

    Missing: Cataracts Usually Congenital
  • Inflammatory Bowel Disease Type 1

    Performing surgery on patients with Crohn's disease is a true challenge due to the elevated risk of complications related to the chronic proinflammatory response. Stenosis is the leading cause of intestinal resection in these patients. The authors present the case of a 50-year-old woman with inflammatory stenosis[…][]

    Missing: Cataracts Usually Congenital
  • Aplastic Anemia

    Aplastic anemia is a disorder of the hematopoietic stem cell that results in a loss of blood cell precursors, hypoplasia or aplasia of bone marrow, and cytopenias in two or more cell lines (RBCs, WBCs, and/or platelets). Symptoms result from anemia, thrombocytopenia (petechiae, bleeding), or leukopenia (infections).[…][]

    Missing: Cataracts Usually Congenital
  • Megaloblastic Anemia

    Catabolism of hemoglobin by the reticuloendothelial cells of the marrow and liver accounts for the increased iron stores and the bilirubinemias [7].[] Bone marrow aspiration is done to rule out a primary bone marrow disorder such as a myelodysplastic syndrome or leukemia and assess iron stores.[] Iron stores vary from being increased before therapy to decreased if iron is consumed during therapy for megaloblastosis.[]

    Missing: Cataracts Usually Congenital

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