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1,821 Possible Causes for Bone Marrow with Increased Iron Stores, Congenital Nonspherocytic Hemolytic Anemia, Hyperuricemia

  • Hereditary Spherocytosis

    Hereditary spherocytosis in the Hispanic population does not often present with severe hyperbilirubinemia. Spectrin and band 3 mutations are most frequent in this population. We present a Hispanic full-term female newborn with early onset significant hyperbilirubinemia without a history of familial hemolytic disorders.[…][ncbi.nlm.nih.gov]

  • Autoimmune Hemolytic Anemia

    Wadsworth, Hyperuricemia and Reticulocytopenia in Association With Autoimmune Hemolytic Anemia in Two Children, American Journal of Clinical Pathology, 10.1309/8DXD-VJT9-UN60[oadoi.org]

  • Glycogen Storage Disease Type 1

    All had hyperuricemia except for one patient with glycogenosis type III.[scholars.northwestern.edu] GSD Ia is characterized by hepatomegaly, hypoglycemia, lactic acidemia, hyperuricemia, hyperlipidemia and short stature.[mayoclinic.pure.elsevier.com] Other features include lactic acidosis, hyperlipidemia, hyperuricemia, and hypoglycemic seizures.[xpertdox.com]

    Missing: Bone Marrow with Increased Iron Stores
  • Pernicious Anemia

    Pernicious anemia (per-NISH-us uh-NEE-me-uh) is a condition in which the body can't make enough healthy red blood cells because it doesn't have enough vitamin B12. Vitamin B12 is a nutrient found in some foods. The body needs this nutrient to make healthy red blood cells and to keep its nervous system working[…][web.archive.org]

    Missing: Congenital Nonspherocytic Hemolytic Anemia
  • Hodgkin Lymphoma

    The endobronchial localization of Hodgkin's disease is a rare entity which is often confused with endobronchial tuberculosis in our setting. We report the case of a 16 years old female who presented with 6 months history of dry cough, hemoptysis, dyspnea, dysphagia and dysphonia. The chest radiography showed a[…][ncbi.nlm.nih.gov]

    Missing: Congenital Nonspherocytic Hemolytic Anemia
  • Sickle Cell Disease

    HbS arises from a mutation substituting thymine for adenine in the sixth codon of the beta-chain gene, GAG to GTG. This causes coding of valine instead of glutamate in position 6 of the Hb beta chain. The resulting Hb has the physical properties of forming polymers under deoxy conditions. It also exhibits changes[…][emedicine.medscape.com]

    Missing: Congenital Nonspherocytic Hemolytic Anemia
  • 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: Hyperuricemia
  • 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]

    Missing: Hyperuricemia
  • Waters-West Syndrome

    Increased metabolic requirements, neoplasia. PATHOLOGY: Microcytic, hypochromic anemia. Low serum iron. Bone-Marrow will show absence of iron.[kumc.edu] […] combined 3 Calabro syndrome Familial glucocorticoid deficiency Chromosome 2q24 microdeletion syndrome Maffucci syndrome Autosomal dominant medullary cystic kidney disease with hyperuricemia[checkrare.com] MalaCards based summary : Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities, is also known as hemolytic anemia lethal congenital nonspherocytic[malacards.org]

  • Congenital Heinz Body Hemolytic Anemia

    Glomerular diseases Glomus tumors Glucocorticoids Glucose-6-phosphate dehydrogenase deficiency Glycogen metabolism Glycolysis and gluconeogenesis Goiter Gonorrhea Gout and hyperuricemia[amboss.com] 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] Another effect of the high turnover state is hyperuricemia (due to catabolism of the purine content of cellular DNA).[web2.iadfw.net]

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