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77 Possible Causes for Burr Cell, Pediatric Disorder

  • Microangiopathic Hemolytic Anemia

    - schistocytes, “burr cells”, “helmet cells” and “triangle cells”. 6.[slideshare.net] Pediatr Blood Cancer 53:537 PubMed CrossRef Google Scholar Buchanan GR (1986) Coagulation disorders in the neonate.[link.springer.com] Supported by a grant from the National Institutes of Health Pediatric Research Loan Repayment Program (National Institute of Neurological Disorders and Stroke, Bethesda, MD[academic.oup.com]

  • Hemolytic Uremic Syndrome

    ., schistocytes, burr cells, or helmet cells) on peripheral blood smear, AND Renal injury (acute onset) evidenced by either hematuria, proteinuria, or elevated creatinine[wwwn.cdc.gov] Renal transplantation in HUS patients with disorders of complement regulation. Pediatr Nephrol 2007;22(1):10–16. PubMed CrossRef Google Scholar 155.[link.springer.com] Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder. Pediatr Nephrol 2007;22(12):2097–2103. PubMed CrossRef Google Scholar 172.[link.springer.com]

  • Fetal Erythroblastosis

    Schistocytes, as a sign of disseminated intravascular coagulation and burr cells, are present, as well as neutropenia and thrombocytopenia.[symptoma.com] Data Cues list assessment data to help you recognize possible pediatric disorders.[books.google.de] If there is extensive disseminated intravascular coagulation, schistocytes and burr cells may be observed and neutropenia and thrombocytopenia may occur.[patient.info]

  • Abetalipoproteinemia

    (burr cells) due to lipid membrane abnormalities Microscopic (histologic) description Marked fat vacuoles in apical villous cytoplasm, normal villi Positive stains Fat stains[pathologyoutlines.com] Adds five new chapters including "Screening and Surveillance of the GI Tract", "Congenital and Developmental Disorders of the GI Tract", "Pediatric Enteropathies of the GI[books.google.de] The molecular genetics of pediatric lipid disorders: recent progress and future research directions. Pediatr Res . 1993 Oct. 34(4):403-15. [Medline] .[emedicine.medscape.com]

  • Hyperlipoproteinemia Type 3

    cells (acanthocytes) A-beta-lipoproteinemia Bassen-Kornzweig Syndrome Burr cells (acanthocytes) Failure to thrive Diarrhea, steatorrhea A-beta-lipoproteinemia Bassen-Kornzweig[memorize.com] Tangier's disease Rare congenital Autosomal Recessive Defect in intestine A-beta-lipoproteinemia Bassen-Kornzweig Syndrome No LDL, VLDL, & Chylomicrons Low Cholesterol & TG Burr[memorize.com]

  • Renpenning Syndrome 1

    . • Burr Cells, Helmet Cells -Mechanical Red Cell Destruction.Pt’s with Prosthetic Valves. • When Vaccinated - Virus Entryinto cells is impaired.[pgneetexam.com] One typical immune reaction in infants and children is PANDAS, or Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infection, another disorder[wikivisually.com] Intended as a quick reference guide to the better known and some less familiar syndromes of neurological interest and developed by a renowned pediatric neurologist with more[books.google.de]

  • Anemia

    Burr cells accompany renal failure and spur cells accompany severe liver disease.[cancertherapyadvisor.com] One of the most common pediatric disorders, anemia has many potential causes. Anemia is often a symptom of a disease rather than a disease itself.[childrenshospital.org] In addition to an experienced, compassionate nurse coordinator (who provides your child and family support, education and care coordination), Nemours’ pediatric blood disorder[nemours.org]

  • Neonatal Isoimmune Neutropenia

    If there is extensive disseminated intravascular coagulation, schistocytes and burr cells may be observed and neutropenia and thrombocytopenia may occur.[patient.info] Succinct, targeted coverage of normal childhood growth and development, as well as the diagnosis, management, and prevention of common pediatric diseases and disorders, make[books.google.it] FBC shows: Anaemia, increased nucleated red blood cells and other red blood cell abnormalities, which may be seen.[patient.info]

  • Langerhans-Cell Histiocytosis

    Langerhans cell histiocytosis was diagnosed after biopsy, and the lesion regressed after cladribine treatment.[ncbi.nlm.nih.gov] PLCH is similar to pediatric histiocytic disorders (Letterer-Siwe disease and Hand-Sch ü ller-Christian disease).[emedicine.medscape.com] Langerhans cell histiocytosis and mastocytoma are clonal disorders of bone-marrow-derived cells, most commonly seen in the pediatric age.[ncbi.nlm.nih.gov]

  • Posthemorrhagic Anaemia of the Newborn

    Other findings include burr cells (uremia), spherocytes (hereditary spherocytosis, autoimmune hemolysis, G6PD deficiency), elliptocytes (hereditary elliptocytosis), schistocytes[aafp.org] Succinct, targeted coverage of normal childhood growth and development, as well as the diagnosis, management, and prevention of common pediatric diseases and disorders, make[books.google.com] , which may suggest the presence of mixed microcytic and macrocytic disease processes (a finding that should be suggested by an elevated red blood cell distribution width)[aafp.org]

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