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98 Possible Causes for Bicytopenia, Pediatric Disorder

  • Gaucher Disease

    Society, Society for Pediatric Research, Society for Inherited Metabolic Disorders Disclosure: Nothing to disclose.[emedicine.medscape.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.medscape.com] , American College of Medical Genetics and Genomics, American Medical Association, American Society of Human Genetics, Society for Inherited Metabolic Disorders, International[emedicine.medscape.com]

  • Adenovirus Infection

    […] encephalopathy, myocarditis, rash) was diagnosed with adenovirus-associated macrophage activation syndrome according to clinical and laboratory parameters (fever, hepatosplenomegaly, bicytopenia[ncbi.nlm.nih.gov]

  • Acute Leukemia

    A 43-year-old female presented with leukocytosis and bicytopenia.[ncbi.nlm.nih.gov] Overall, patients with Down syndrome compose approximately 10% of pediatric patients with AML.[clinicaladvisor.com] Initial CBC showed bicytopenia, elevated blood urea, creatinine, and serum uric acid, while abdominal ultrasonography revealed bilateral renal enlargement.[ncbi.nlm.nih.gov]

  • Familial Neutropenia

    RCUD and MDS-U categories in 196 patients with less than 5% marrow blasts, Maassen et al. found 28% RA, 6% RT, 13% RN, 20% patients with no cytopenia, and 34% patients with bicytopenia[mjhid.org] […] physician involved in the diagnosis of pediatric bone marrow disorders.[books.google.de] […] suspected pediatric age Corneal disorders ICD9CM Coronary artery disease unstable Cough chronic Creatine kinase elevation Cushings syndrome Cutaneous microvascular occlusion[books.google.com]

  • Congenital Neutropenia

    Falk PM, Rich K, Feig S, Stiehm ER, Golde DW, Cline MJ (1977) Evaluation of congenital neutropenic disorders by in vitro bone marrow culture.[link.springer.com] At age 8, on check-up, had mild bicytopenia (anemia and thrombocytopenia). Was followed with bone marrow aspirates and biopsies.[ascopubs.org] This case report emphasizes the role of periodontists and pediatric dentists in the diagnosis of diseases linked with neutrophil and other systemic disorders and highlights[ncbi.nlm.nih.gov]

  • Hypocupremia

    Bone marrow aspirate done to evaluate the cause of bicytopenia revealed trilineage dysplasia.[read.qxmd.com] , University of Texas Southwestern Medical Center; Clinical Director of Hematology, Pauline Allen Gill Center for Cancer and Blood Disorders, Children’s Medical Center Dallas[emedicine.staging.medscape.com] Copper deficiency usually presents with bicytopenia (neutropenia and anemia), but severe pancytopenia has been observed in some cases, especially those patients on TPN.[haematologica.org]

  • Acute Myelocytic Leukemia

    In contrast to patients with RA and only dyserythropoiesis, patients with multilineage dysplasia have bicytopenia or pancytopenia, a higher incidence of cytogenetic abnormalities[dx.doi.org] Hasle H: Myelodysplastic and myeloproliferative disorders in children. Curr Opin Pediatr 19 (1): 1-8, 2007.[northshore.org] Webb, Acute Myeloid Leukemia and Myelodysplastic Disorders, Pediatric Hematology and Oncology, (95-108), (2010).[doi.org]

  • Systemic Mastocytosis

    Although the patient responded to the treatment, the relapse with splenomegaly and bicytopenia was observed after 10 months.[ncbi.nlm.nih.gov] In Romania, the number of the diagnosed patients with mast cell disorders is 252, of which 180 adults and 73 pediatric patients.[medichub.ro] […] myeloid disorders), and the response to therapy.[ecnm.net]

  • Adenosine Deaminase Deficiency

    Because patient 5 had bicytopenia during admission, a bone marrow aspiration was performed and the diagnosis was myelofibrosis.[jrheum.org] Adenosine deaminase severe combined immunodeficiency (ADA-SCID) is a rare, inherited, pediatric disorder that is often fatal when left untreated.[leadiant.com] Pediatr Neurol. 2007 Sep;37(3):218-21. Nyhan WL. Disorders of purine and pyrimidine metabolism. Mol Genet Metab. 2005 Sep-Oct;86(1-2):25-33. Review.[ghr.nlm.nih.gov]

  • Erythema Infectiosum

    Leukophagocytosis in human parvovirus B19-induced transient bicytopenia in a healthy child. Acta Paediatr. Jpn. 38 : 278 -281. Walsh, K. J., R. D. Armstrong, and A. M.[cmr.asm.org] […] symptoms in infants, children, and young adults through images of common and unusual presenting features for over 300 pediatric disorders.[euro-libris.ro] Continue reading the main story But the disorders that go by numbers are few and belong to pediatrics. There are as many as six, all with somewhat similar rashes.[nytimes.com]

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