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74 Possible Causes for Burr Cell, Pediatric Disorder

  • 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] 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] Title Other Names: HUS; Acute renal failure, thrombocytopenia, and microangiopathic hemolytic anemia associated with distorted erythrocytes ('burr cells') Categories: Hemolytic[rarediseases.info.nih.gov]

  • 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] -schistocytes -fragements -burr cells -microspherocytes What are some causes of microangiopathic hemolytic anemia?[quizlet.com]

  • 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]

  • 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] Davidson and Emile Levy, Congenital Disorders of Lipid Transport, Textbook of Pediatric Gastroenterology, Hepatology and Nutrition, 10.1007/978-3-319-17169-2_38, (437-444)[doi.org]

  • 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]

  • Becker Muscular Dystrophy

    A R Burr and J D Molkentin, Genetic evidence in the mouse solidifies the calcium hypothesis of myofiber death in muscular dystrophy, Cell Death & Differentiation, 10.1038[doi.org] Little is known about parental motivations and expectations for clinical trials for rare pediatric disorders.[ncbi.nlm.nih.gov] Breath stacking in children with neuromuscular disorders. Pediatr Pulmonol. 2013 Aug 16. [Medline].[emedicine.medscape.com]

  • Langerhans-Cell Histiocytosis

    Langerhans cell histiocytosis (LCH) developing in a burr hole site for chronic subdural hematoma is extremely rare.[ncbi.nlm.nih.gov] Ting-Wen An Lee, Radhika Muzumdar and Paul Saenger, Growth Disorders, Textbook of Clinical Pediatrics, 10.1007/978-3-642-02202-9_386, (3739-3757), (2012).[doi.org] Langerhans cell histiocytosis was diagnosed after biopsy, and the lesion regressed after cladribine treatment.[ncbi.nlm.nih.gov]

  • Congenital Liver Cirrhosis

    It is characterized by microangiopathic hemolysis with burr cells and schistocytes on peripheral smear; elevated liver enzyme levels, with aspartate transaminase (AST) exceeding[clevelandclinicmeded.com] Contact the Pediatric Surgery Service at: 617-726-0270 Pediatric Liver and Biliary Disease Center Pediatric Patients Only The Pediatric Liver and Biliary Disease Center at[massgeneral.org] ARPKD, the most common pediatric ciliopathy, is characterized by cystic degeneration of the kidneys and congenital hepatic fibrosis of the liver.[clinicaltrials.gov]

  • Spinal Muscular Atrophy

    ., Burres, N., Feng, L., Whitney, M., Roemer, K. and Tsien, R.Y. ( 1998 ) Quantitation of transcription and clonal selection of single living cells wih β-lactamase as a reporter[doi.org] The Pediatric SMA Clinical Research Center, which operates conjointly with the Pediatric Neuromuscular Clinic at Columbia University, is organized according to a team model[columbiasma.org] Our pediatric endocrinologists provide family-centered care for children and adolescents with type 1 and type 2 diabetes, adrenal and thyroid disorders, gender disorders,[dukechildrens.org]

  • 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]

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