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6,181 Possible Causes for Pediatric Disorder, Progressive or Intermittent Jaundice, Reticulocytes Increased

  • Hereditary Spherocytosis

    Reticulocyte count: Increased Treatment: Splenectomy is indicated for moderate to severe cases, but not mild cases.[medical-labs.net] The 2003 Healthcare Cost and Utilization Project (HCUP) Kids’ Inpatient Database (KID), a robust and widely used measure of pediatric disorders, has estimated that the number[touchoncology.com] Hans-Christoph Rossbach, THE RULE OF FOUR: A SYSTEMATIC APPROACH TO DIAGNOSIS OF COMMON PEDIATRIC HEMATOLOGIC AND ONCOLOGIC DISORDERS, Fetal and Pediatric Pathology, 24, 6[doi.org]

    Missing: Progressive or Intermittent Jaundice
  • Congenital Dyserythropoietic Anemia

    On this treatment, hemoglobin and reticulocytes increased and transfusions became unnecessary.[ncbi.nlm.nih.gov] Hereditary Elliptocytosis and Related Disorders Pediatric Lead Toxicity Pediatric Megaloblastic Anemia Pediatric Myelodysplastic Syndrome Sickle Cell Anemia Transient Erythroblastopenia[emedicine.medscape.com] The reticulocyte count was always low, in spite of the increased erythropoietic activity. A beta-thalassemia trait inherited from the mother was demonstrated.[ncbi.nlm.nih.gov]

    Missing: Progressive or Intermittent Jaundice
  • Fetal Erythroblastosis

    He or she will be anemic, with increased reticulocyte count, anisocytosis, spherocytosis, and young (nucleated, immature) red blood cells released into circulation.[symptoma.com] Data Cues list assessment data to help you recognize possible pediatric disorders.[books.google.de] Peripheral blood morphology shows increased reticulocytes. Erythroblasts (also known as nucleated red blood cells) occur in moderate and severe disease.[moondragon.org]

    Missing: Progressive or Intermittent Jaundice
  • Sickle Cell Disease

    With each course, fetal reticulocytes increased within 48-72 h, peaked in 7-11 d, and fell by 18-21 d.[doi.org] Elder and Jeremie Heath Estepp, Hematologic Disorders of the Eye, The Eye in Pediatric Systemic Disease, 10.1007/978-3-319-18389-3_11, (295-325), (2017).[doi.org] Center, Children's Healthcare of Atlanta, Emory University, Atlanta, Georgia. 4 Department of Pediatrics, Yale University, New Haven, Connecticut. 5 Department of Laboratory[ncbi.nlm.nih.gov]

    Missing: Progressive or Intermittent Jaundice
  • Congenital Hemolytic Anemia

    After partial splenectomy, children overall had decreased transfusion requirements, increased hematocrits, decreased bilirubin levels, decreased reticulocyte counts, and elimination[ncbi.nlm.nih.gov] Hemolytic anemia Hereditary elliptocytosis Hereditary pyropoikilocytosis Red cell membrane disorder Pediatrics, Perinatology, and Child Health Hematology Oncology Cite this[scholars.northwestern.edu] As a result of splenectomy, reticulocyte counts often increase and transfusion needs are reduced.[orpha.net]

    Missing: Progressive or Intermittent Jaundice
  • Hemolytic Uremic Syndrome

    reticulocytes reduced haptoglobins increased LDH unconjugated hyperbilirubinaemia with urinary urobilinogen variable neutrophilia increased urea and creatinine levels (greater[lifeinthefastlane.com] Rekha Hans, Satya Prakash, Ratti Ram Sharma and Neelam Marwaha, Role of therapeutic apheresis in pediatric disorders, Pediatric Hematology Oncology Journal, 10.1016/j.phoj[doi.org] L-lactate dehydrogenase level Leukocytosis Negative Coombs’ test Proteinuria on urinalysis Reticulocyte count moderately elevated Stool culture positive for Shiga toxin–roducing[aafp.org]

    Missing: Progressive or Intermittent Jaundice
  • Gaucher Disease

    Society, Society for Pediatric Research, Society for Inherited Metabolic Disorders Disclosure: Nothing to disclose.[emedicine.com] , Society for Pediatric Research, Society for the Study of Inborn Errors of Metabolism Disclosure: Serve(d) as a director, officer, partner, employee, advisor, consultant[emedicine.com] , American College of Medical Genetics and Genomics, American Medical Association, American Society of Human Genetics, Society for Inherited Metabolic Disorders, International[emedicine.com]

    Missing: Progressive or Intermittent Jaundice
  • Pyruvate Kinase Deficiency

    Char10C mice also display a reduction in anemia phenotypes associated with the PklrG338D mutation including decreased splenomegaly, decreased circulating reticulocytes, increased[ncbi.nlm.nih.gov] Stephen Rogers, Manuel Silva and Allan Doctor, Hematologic Disorders, Studies on Pediatric Disorders, 10.1007/978-1-4939-0679-6_21, (349-369), (2014).[doi.org] As a result of splenectomy, reticulocyte counts often increase and transfusion needs are reduced.[orpha.net]

    Missing: Progressive or Intermittent Jaundice
  • Meckel Diverticulum

    disorders.[books.google.ro] BMC Endocr Disord. 2015 Nov 26. 15:72. [Medline]. [Full Text].[emedicine.medscape.com] Benefit from authoritative guidance on genetic disorders and dysmorphic conditions, neonatology, developmental-behavioral pediatrics, allergy and immunology, conditions of[books.google.ro]

    Missing: Progressive or Intermittent Jaundice
  • Glycogen Storage Disease Type 1

    Nelson Textbook of Pediatrics. 16th ed. Philadelphia: Saunders; 2000. p. 405. 6. Bickel H, Manz F.[journalofpediatriccriticalcare.com] […] patients with inheritable metabolic disorders.[ojrd.biomedcentral.com] Hereditary tubular disorders of the Fanconi type and the idiopathic Fanconi syndrome. Prog Clin Biol Res. 1989;305:111–135. 7.[journalofpediatriccriticalcare.com]

    Missing: Progressive or Intermittent Jaundice

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