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Recommended Conferences

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  • 8th International Conference on Blood Cancer & Treatment June 26-27, 2017 London, UK
    June 26-27, 2017 London, UK
  • International Conference on Hematology and Oncology June 29-July 01, 2017 Bangkok, Thailand
    June 29-July 01, 2017 Bangkok, Thailand
  • 9th International Conference on Hematology November 02-03, 2017 Las Vegas, USA
    November 02-03, 2017 Las Vegas, USA
  • 11th International Conference on Leukemia and Hematologic Oncology December 04-05, 2017 Madrid, Spain
    December 04-05, 2017 Madrid, Spain
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Relevant Topics

  • Pediatric white blood cell disorders

    Pathophysiology

    Body produces white blood cells (leukocytes), which help fight bacterial infections, viruses and fungi. If your child has too few or too many white blood cells, in general, here's what it means: Low white blood cell count (leukopenia) means having too few leukocytes circulating in the blood. A long-term low white blood cell count increases the risk of infections and may be caused by a number of different diseases and conditions.

  • Pediatric white blood cell disorders

    Disease statistics

    Sensitivity and specifity in receiver operating characteristics, and positive and negative predictive value of CRP and white blood cell count were compared in 195 critically ill preterm and term newborns clinically suspected of infection. Blood cultures were positive in 33 cases.

  • Pediatric white blood cell disorders

    Treatment

    Treatments for white blood cell disorders depend on several factors, including: The type of disorder, The extent of the disorder, Your child’s overall health, Your child’s response to treatment, Your preferences Our treatments for your child’s white blood cell disorder may include: Chemotherapy, Radiation, Antibiotics, Colony-stimulating factors (these increase the body’s production of blood cells), Drugs to suppress the immune system Stem cell transplantation may be useful for some types of severe white blood cell disorders, particularly those caused by bone marrow problems.

  • Pediatric white blood cell disorders

    Research

    From 1988 to 1998. Patients were followed for an average of 4.2 ± 2.0 years. Age-specific prevalence and incidence rates of CVA in patients with the common genotypes of sickle cell disease were determined, and the effects of hematologic and clinical events on the risk of CVA were analyzed. The highest rates of prevalence of CVA (4.01%) and incidence (0.41 per 100 patient-years) were in sickle cell anemia (SS) patients, but CVA occurred in all common genotypes. The incidence of infarctive CVA was lowest in SS patients 20 to 27 years of age and higher in children and older patients.

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