@article{3120964,
    title = "Massive Splenic Infarction and Autosplencetomy: First Presentation of Homozygous Sickle Cell Disease in a Toddler",
    author = "Krepis, P. and Maritsi, D.N. and Tsolia, M.N. and Vakaki, M. and Kossiva, L.",
    journal = "Journal of Pediatric Hematology / Oncology",
    year = "2020",
    volume = "42",
    number = "5",
    pages = "371-372",
    publisher = "Lippincott Williams and Wilkins",
    issn = "1077-4114, 1536-3678",
    doi = "10.1097/MPH.0000000000001698",
    keywords = "C reactive protein;  ceftriaxone;  creatinine;  hemoglobin;  hemoglobin beta chain;  lactate dehydrogenase;  procalcitonin, abdominal distension;  abdominal pain;  abdominal tenderness;  bacterial infection;  case report;  child;  childhood disease;  clinical article;  Congo;  creatinine blood level;  dehydration;  deterioration;  diarrhea;  distress syndrome;  echography;  electrophoresis;  erythrocyte transfusion;  female;  gastroenteritis;  gene mutation;  genetic screening;  hematocrit;  hemodynamics;  hospital admission;  human;  Letter;  lymphocyte count;  neutrophil count;  outcome assessment;  platelet count;  preschool child;  priority journal;  reticulocyte count;  sickle cell anemia;  skin turgor;  spleen infarction;  splenectomy;  urea nitrogen blood level;  vomiting;  complication;  homozygote;  infant;  pathology;  prognosis;  sickle cell anemia;  sickle cell trait;  spleen infarction, Anemia, Sickle Cell;  Female;  Homozygote;  Humans;  Infant;  Prognosis;  Sickle Cell Trait;  Splenic Infarction"
}