نتایج جستجو برای: hematologic abnormalities

تعداد نتایج: 122867  

Journal: :Archives of neurology 2003
Peter Hedera John K Fink Paula L Bockenstedt George J Brewer

OBJECTIVE To describe a patient with idiopathic zinc overload without an identifiable source and secondary copper deficiency causing myelopolyneuropathy and pancytopenia. DESIGN Case report. PATIENT AND RESULTS A 46-year-old man presented with severe bone marrow suppression and subsequently developed progressive myelopathy with sensory ataxia. No identifiable cause of myelopathy was detecte...

Journal: :Blood 1974
T Isobe E F Osserman

The clinical, hematologic, and immunoglobulin features of a new form of plasma cell dyscrasia (deleted H and L chain disease) are described. The clinical manifestations are periodic fever and weakness, lymphadenopathy, and hepatosplenomegaly. The hematologic abnormalities are anemia, leukopenia, lymphocytosis, thrombocytopenia, and increased plasma cells in lymph nodes and bone marrow. The prot...

Journal: :Blood 1992
F Louache A Henri A Bettaieb E Oksenhendler G Raguin M Tulliez W Vainchenker

A number of hematologic abnormalities, including cytopenias, have been observed in patients with human immunodeficiency virus (HIV) infection. To elucidate their mechanisms, a group of 27 patients with HIV-1 infection was studied. In all patients, a marked reduction of in vitro colony formation by erythroid, granulomacrophagic, and megakaryocytic bone marrow progenitors was observed in comparis...

Journal: :Blood 1983
H J Tanke P H Rothbarth J M Vossen G J Koper J S Ploem

Reticulocytes in fixed human blood samples were stained for RNA with the fluorescent dye pyronin Y and measured by flow cytometry. The resulting relative frequency distributions of the RNA fluorescence intensities concurred with the different stages in maturation from early reticulocytes to mature red cells. A computer program was written to calculate from these frequency distributions the rela...

2004
David P. Steensma Douglas R. Higgs Chris A. Fisher Richard J. Gibbons

Acquired somatic mutations in ATRX, an X-linked gene encoding a chromatinassociated protein, were recently identified in 4 patients with the rare subtype of myelodysplastic syndrome (MDS) associated with thalassemia (ATMDS). Here we describe a series of novel point mutations in ATRX detected in archival DNA samples from marrow and/or blood of patients with ATMDS by use of denaturing high-perfor...

Journal: :Blood 2002
Nicole Dastugue Marina Lafage-Pochitaloff Marie-Pierre Pagès Isabelle Radford Christian Bastard Pascaline Talmant Marie Joelle Mozziconacci Claude Léonard Christelle Bilhou-Nabéra Christine Cabrol Anne-Marie Capodano Pascale Cornillet-Lefebvre Michel Lessard Francine Mugneret Christine Pérot Sylvie Taviaux Odile Fenneteaux Eliane Duchayne Roland Berger

To draw the cytogenetic profile of childhood and adult acute megakaryoblastic leukemia (M7), the Groupe Français de Cytogénétique Hématologique collected 53 cases of M7 (30 children and 23 adults). Compared to other acute myeloid leukemias, M7 is characterized by a higher incidence of abnormalities, a higher complexity of karyotypes, and a different distribution of abnormalities among children ...

2005
Takashi Isobe Elliott F. Osserman

The clinical, hematologic, and immunoglobulin features of a new form of plasma cell dyscrasia (deleted H and L chain disease) are described. The clinical manifestations are periodic fever and weakness, lymphadenopathy, and hepatosplenomegaly. The hematologic abnormalities are anemia, leukopenia, lymphocytosis, thrombocytopenia, and increased plasma cells in lymph nodes and bone marrow. The prot...

2006
Shih-Hsiang Lo Chang-Chuan Chan Wei-Chin Chen Jung-Der Wang

CONTEXT Although there are ample data on the respiratory effects of exposure to fire extinguisher gas, the potential hematologic effects have not been fully documented. We conducted this study to determine the possible etiologic agent(s) for a decrease in red blood cells among community residents in Taipei, Taiwan, after they were exposed to leakage of mixed fire extinguishants containing bromo...

Journal: :Blood 1995
W G Beamer S C Pelsue L D Shultz J P Sundberg J E Barker

Flaky skin (gene symbol fsn) is an autosomal recessive mutation that causes pleiotropic effects of anemia, papulosquamous skin disorder, and gastric forestomach hyperplasia. In this report, we assign fsn to distal chromosome 17 and characterize the anemia. The decrease in hematocrit levels and red blood cell counts is significant and persists throughout life in fsn/fsn mice. There is compensato...

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