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73 Possible Causes for Hematocrit Decreased, Neonatal Hyperbilirubinemia, Reticulocytes Increased

  • Hereditary Spherocytosis

    neonatal hyperbilirubinemia.[] Reticulocyte count: Increased Treatment: Splenectomy is indicated for moderate to severe cases, but not mild cases.[] A complete blood count (CBC) may show increased reticulocytes, a sign of increased red blood cell production, and decreased hemoglobin and hematocrit.[]

  • Thalassemia Minor

    Abstract Infants on this island are known to have higher incidences of neonatal hyperbilirubinemia and alpha-thalassemia minor than Caucasians.[] […] count Normal May be slightly increased Slightly increased ( Mildly increased (5 - 10%) Mildly increased Hb electrophoresis Normal pattern Decreased amount of Hb A Variable[] Abstract Patients with heterozygous beta-thalassemia minor have a decreased hematocrit (HCT).[]

  • Congenital Hemolytic Anemia

    He required phototherapy for neonatal jaundice.[] After partial splenectomy, children overall had decreased transfusion requirements, increased hematocrits, decreased bilirubin levels, decreased reticulocyte counts, and elimination[] As a result of splenectomy, reticulocyte counts often increase and transfusion needs are reduced.[]

  • Sickle Cell Disease

    jaundice, mesothelioma, unintentional suffocation, pulmonary aspiration and foreign body in trachea or lung, and foreign body in other part of body.[] With each course, fetal reticulocytes increased within 48-72 h, peaked in 7-11 d, and fell by 18-21 d.[] (p 0.001), while hemoglobin and hematocrit remained stable.[]

  • Pyruvate Kinase Deficiency

    We report an infant with neonatal hyperbilirubinemia due to pyruvate kinase deficiency.[] Char10C mice also display a reduction in anemia phenotypes associated with the PklrG338D mutation including decreased splenomegaly, decreased circulating reticulocytes, increased[] As a result of splenectomy, reticulocyte counts often increase and transfusion needs are reduced.[]

  • Cooley's Anemia

    Children may develop dramatic, often life threatening drops in hematocrit with reticulocyte counts of nearly zero.[] The differential white blood count shows a decrease in most types of cells but not lymphocytes .[] This "aplastic crisis" often requires emergent transfusion support The effectiveness of present effective strategies has increased the life spans of patients with thalassaemia[]

  • Glycogen Storage Disease Type 1

    Glycogen storage disease type 1 (GSD1) is an inborn error of metabolism caused by deficiency of glucose-6-phosphatase, the enzyme catalysing the conversion of glucose-6-phosphate (G6P) to glucose. GSD1 is associated with severe hyperlipidaemia and hepatic steatosis. The underlying mechanisms responsible for these[…][]

  • Congenital Dyserythropoietic Anemia

    These results confirm the authors' previous findings and add neonatal manifestations not previously described, particularly hyperbilirubinemia and thrombocytopenia.[] On this treatment, hemoglobin and reticulocytes increased and transfusions became unnecessary.[] Following delivery the infant had serial blood counts performed over a 6-week period, which noted a steady decrease in her hematocrit to 16%.[]

  • Hereditary Elliptocytosis

    Neonatal hyperbilirubinemia and severe anemia in the first few months of life are the typical presenting signs.[] His hemoglobin is now practically normal, but he still has a slight but persistent reticulocyte increase.[] Post-splenectomy, patients with HE or HPP exhibit increased hematocrit, decreased reticulocyte counts, and improved clinical symptoms.[]

  • Fetal Erythroblastosis

    Fetal and neonatal edition, 2018 May 25 [PubMed] Bilirubin Albumin Binding and Unbound Unconjugated Hyperbilirubinemia in Premature Infants., Amin SB,Wang H,, The Journal[] He or she will be anemic, with increased reticulocyte count, anisocytosis, spherocytosis, and young (nucleated, immature) red blood cells released into circulation.[] Both the newborns further showed progressive decrease in hematocrit (HCT) and later developed hepatosplenomegaly.[]

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