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2,121 Possible Causes for Bone Marrow with Increased Iron Stores, Glycogen Storage Disease Type 1, Polychromasia in Peripheral Blood Smear

  • Autoimmune Hemolytic Anemia

    Peripheral blood smear showed polychromasia and spherocytosis. Haptoglobin level was 0.06 g/L ( N 0.16-2). Both hemoglobin electrophoresis and G6PD level were normal.[jahjournal.org] -Red cell morphology on review of the peripheral blood smear may demonstrate microspherocytes and polychromasia which are suggestive of a reactive reticulocytosis.[oncologynurseadvisor.com] Red blood cell agglutination, polychromasia, target cells and spherocytes were seen on a peripheral smear.[jmedicalcasereports.com]

  • Pyruvate Kinase Deficiency

    In PFK deficiency (glycogen storage disease type VII), clinical hallmarks are male predominance with early onset gout, compensated hemolytic process, and prominent myopathy[ommbid.mhmedical.com] Peripheral blood smear showed polychromasia, anisocytosis, tear drop cells, fragmented eyrtrocytes, and target cells.[ncbi.nlm.nih.gov]

  • Hemochromatosis

    […] variant in the BCS1L gene; relevant for Finnish descent Gaucher Disease Type 1 3 variants in the GBA gene; relevant for Ashkenazi Jewish descent Glycogen Storage Disease Type[23andme.com] Ia 1 variant in the G6PC gene; relevant for Ashkenazi Jewish descent Glycogen Storage Disease Type Ib 2 variants in the SLC37A4 gene Hereditary Fructose Intolerance 4 variants[23andme.com] […] relevant for Arab, Armenian, Sephardic Jewish, Turkish descent Fanconi Anemia Group C 3 variants in the FANCC gene; relevant for Ashkenazi Jewish descent GRACILE Syndrome 1[23andme.com]

    Missing: Polychromasia in Peripheral Blood Smear
  • Inflammatory Bowel Disease

    BACKGROUND: Inflammatory bowel disease (IBD)-like conditions in glycogen storage disease (GSD) type Ib have been predominantly described in children.[ncbi.nlm.nih.gov] RTEL1 SH2D1A SH2D1A deficiency (XLP1) SH2 domain protein 1A SH2D1A SLC37A4 Glycogen storage disease type 1b glucose-6-phosphate transporter 1 G6PT1 STAT1 STAT1 deficiency[invitae.com] RAG2 RAG 2 deficiency recombinase activating gene 2 RAG2 RTEL1 AR-DKC due to regulator of telomere elongation (RTEL1) deficiency regulator of telomere elongation helicase 1[invitae.com]

    Missing: Polychromasia in Peripheral Blood Smear
  • Paroxysmal Cold Hemoglobinuria

    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] storage disease グリコーゲン蓄積症,糖原病(0a型) glycogen storage disease (type 0a) グリコーゲン蓄積症,糖原病(0b型) glycogen storage disease (type 0b) グリコーゲン蓄積症,糖原病(I型) glycogen storage disease (type[jsge.or.jp] Tests include complete blood count (CBC) and peripheral smear.[emedicine.com]

  • Inflammatory Bowel Disease Type 1

    Inflammatory bowel disease in glycogen storage disease type Ib. J Pediatr 1986; 109 : 55-59 PubMed 27 Sanderson IR, Bisset WM, Milla PJ, Leonard JV.[web.archive.org] Patients with glycogen storage disease (GSD) Ib[ 26, 27 ], chronic granulomatous disease (CGD)[ 28 ], Chediak Higashi syndrome[ 29 ], Hermansky-Pudlak syndrome[ 30 ] leukocyte[doi.org] Association of glycogen storage disease 1b and Crohn disease: results of a North American survey.[ncbi.nlm.nih.gov]

    Missing: Polychromasia in Peripheral Blood Smear
  • Acquired Sideroblastic Anemia

    It is characterized by 15% or more ringed sideroblasts in the bone marrow, 1 increased bone marrow iron stores 2 and less than 5% blasts in the bone marrow or less than 1%[nature.com] Blood Smear Peripheral blood smear images .[imagebank.hematology.org] […] on bone marrow examination.[thebigl.co]

    Missing: Glycogen Storage Disease Type 1
  • Sideroblastic Anemia

    Blood Smear Peripheral blood smear images .[imagebank.hematology.org] Diagnosis made by examination of the bone marrow 1- Marked erythoid hyperplasia; a sign of ineffective erytropoieses 2- Prussian blue iron strain stores bone marrow shows[quizlet.com] increased iron stores, ringed sideroblasts 15% of marrow erythroblasts, identify with iron stain on marrow smear, has nucleus completely or partially (at least one third[pathologyoutlines.com]

    Missing: Glycogen Storage Disease Type 1
  • Chronic Acquired Pure Red Cell Aplasia

    There was also increase in myeloid-erythroid ratio (8:1), platelet series was normal. Marrow iron stores were normal.[ijmstrust.in] storage disease グリコーゲン蓄積症,糖原病(0a型) glycogen storage disease (type 0a) グリコーゲン蓄積症,糖原病(0b型) glycogen storage disease (type 0b) グリコーゲン蓄積症,糖原病(I型) glycogen storage disease (type[jsge.or.jp] storage disease due to aldolase A deficiency Glycogen storage disease due to muscle phosphofructokinase deficiency Glycogen storage disease due to phosphoglycerate kinase[se-atlas.de]

  • Congenital Hemolytic Anemia

    Laboratory The review of the peripheral blood smear revealed no evidence of the schistocytes or fragmented red cells.[medcraveonline.com] blood smear of Congenital Hemolytic Anemia Describe the extent of central pallor of a normal RBC T/F: There is increased reticulocytosis and polychromasia in Congenital Hemolytic[brainscape.com] Hemosiderinuria is seen in chronic intravascular hemolysis. 4) Examination of blood smear: Careful examination of peripheral blood smear by an experienced person provides[bioline.org.br]

    Missing: Glycogen Storage Disease Type 1

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