Please use this identifier to cite or link to this item: http://www.repositorio.ufc.br/handle/riufc/10943
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dc.contributor.authorChaves, Filipe Nobre-
dc.contributor.authorFonteles, Cristiane Sá Roriz-
dc.contributor.authorCarvalho, Francisco Sanuel Rodrigues-
dc.contributor.authorRibeiro, T. R.-
dc.contributor.authorPereira, Karuza Maria Alves-
dc.contributor.authorCosta, Fábio Wildson Gurgel-
dc.date.accessioned2015-03-13T16:04:47Z-
dc.date.available2015-03-13T16:04:47Z-
dc.date.issued2014-
dc.identifier.citationCHAVES, F. N. et al. An adult blind man presenting severe impairment of the right finger, ecchymosis in the thorax region, and haemorrhagic blisters on the oral mucosa. Case Reports in Dentistry, New York, v. 24, p. 1-5, 2014.pt_BR
dc.identifier.issn2090-6447-
dc.identifier.urihttp://www.repositorio.ufc.br/handle/riufc/10943-
dc.description.abstractThrombocytopenia is defined as a reduced platelet count within blood (<100 9 109 units/L),1 generating a primary haemostatic defect.2 This condition may be observed in diseases associated with (i) impaired platelet production (e.g. aplastic anaemia, myelodysplastic syndrome, chemotherapy), and (ii) increased splenic sequestration (e.g. splenomegaly, disseminated intravascular coagulation, thrombotic microangiopathy).1,2 Immune thrombocytopenic purpura (ITP) consists of an acquired immune-mediated disorder with severe dermatological manifestations in which auto-antibodies establish a direct link with specific glycoproteins expressed on platelet surfaces, such as IIb-IIIa and Ib-IX, promoting platelet destruction by macrophages from the reticuloendothelial system.pt_BR
dc.language.isoenpt_BR
dc.publisherCase Reports in Dentistrypt_BR
dc.subjectEquimosept_BR
dc.subjectMucosa Bucalpt_BR
dc.titleAn adult blind man presenting severe impairment of the right finger, ecchymosis in the thorax region, and haemorrhagic blisters on the oral mucosapt_BR
dc.typeArtigo de Periódicopt_BR
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