Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/200278
Full metadata record
DC FieldValueLanguage
dc.contributor.CRUESPUNIVERSIDADE DE ESTADUAL DE CAMPINASpt_BR
dc.typeArtigo de periódicopt_BR
dc.titleDiagnosis Of Scott Syndrome In Patient With Bleeding Disorder Of Unknown Cause.pt_BR
dc.contributor.authorFlores-Nascimento, Mariane Cpt_BR
dc.contributor.authorOrsi, Fernanda L Apt_BR
dc.contributor.authorYokoyama, Ana Ppt_BR
dc.contributor.authorPereira, Fernanda Gpt_BR
dc.contributor.authorLorand-Metze, Irenept_BR
dc.contributor.authorDe Paula, Erich Vpt_BR
dc.contributor.authorCastro, Vagnerpt_BR
dc.contributor.authorAnnichino-Bizzacchi, Joyce Mpt_BR
unicamp.authorMariane C Flores-Nascimento, Hematology and Hemotherapy Center, State University of Campinas (UNICAMP), Campinas, Sao Paulo, Brazil. flores_mariane@yahoo.com.brpt_BR
unicamp.author.externalFernanda L A Orsi,pt
unicamp.author.externalAna P Yokoyama,pt
unicamp.author.externalFernanda G Pereira,pt
unicamp.author.externalIrene Lorand-Metze,pt
unicamp.author.externalErich V De Paula,pt
unicamp.author.externalVagner Castro,pt
unicamp.author.externalJoyce M Annichino-Bizzacchi,pt
dc.subjectAdolescentpt_BR
dc.subjectBlood Coagulation Disorderspt_BR
dc.subjectBlood Coagulation Testspt_BR
dc.subjectBlood Plateletspt_BR
dc.subjectFemalept_BR
dc.subjectHumanspt_BR
dc.subjectSyndromept_BR
dc.description.abstractScott syndrome is a rare bleeding disorder due to an impaired exposure of phosphatidilserine on the platelet membrane, compromising the platelet procoagulant activity, thrombin generation and, thus, the clot formation. We report a case of a 17-year-old female adolescent with bleeding episodes of unknown cause. She had normal coagulation, but altered platelet aggregation under arteriolar flow, indicating platelet dysfunction. Furthermore, the expression of Annexin V was markedly reduced and the diagnosis of Scott syndrome was established. She was treated with platelet transfusions and demonstrated a clinical improvement. Scott syndrome may be investigated in cases with bleeding history and normal coagulation tests.en
dc.relation.ispartofBlood Coagulation & Fibrinolysis : An International Journal In Haemostasis And Thrombosispt_BR
dc.relation.ispartofabbreviationBlood Coagul. Fibrinolysispt_BR
dc.date.issued2012-Janpt_BR
dc.identifier.citationBlood Coagulation & Fibrinolysis : An International Journal In Haemostasis And Thrombosis. v. 23, n. 1, p. 75-7, 2012-Jan.pt_BR
dc.language.isoengpt_BR
dc.description.volume23pt_BR
dc.description.firstpage75-7pt_BR
dc.rightsfechadopt_BR
dc.sourcePubMedpt_BR
dc.identifier.issn1473-5733pt_BR
dc.identifier.doi10.1097/MBC.0b013e32834d0c81pt_BR
dc.identifier.urlhttp://www.ncbi.nlm.nih.gov/pubmed/22027759pt_BR
dc.date.available2015-11-27T13:29:03Z-
dc.date.accessioned2015-11-27T13:29:03Z-
dc.description.provenanceMade available in DSpace on 2015-11-27T13:29:03Z (GMT). No. of bitstreams: 0 Previous issue date: 2012en
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/200278-
dc.identifier.idPubmed22027759pt_BR
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.