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dc.contributor.authorPerez, Amanda Vilaverdept_BR
dc.contributor.authorOliveira Filho, Cilomar Martins dept_BR
dc.contributor.authorPazinato, Tássia Cividanespt_BR
dc.contributor.authorSilva, Mariana Sbaraini dapt_BR
dc.contributor.authorValério, Edimárlei Gonsalespt_BR
dc.contributor.authorAmaral, Sheila Nogueira dopt_BR
dc.contributor.authorGrossi, Fernanda Santospt_BR
dc.contributor.authorVettori, Daniela Vanessapt_BR
dc.contributor.authorVettorazzi, Janetept_BR
dc.date.accessioned2021-05-13T04:26:53Zpt_BR
dc.date.issued2019pt_BR
dc.identifier.issn2160-8806pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/220848pt_BR
dc.description.abstractBackground: Bernard-Soulier Syndrome (BSS) is a rare autosomal recessively inherited bleeding disorder of platelet function. Pregnancy in BSS is associated with a high risk of serious bleeding for both mother and neonate, and current data show no consensual approach. Aim: To report the case of a pregnant woman with BSS, in order to provide more information about management of these cases. Case Presentation: This case report describes a successful pregnancy outcome in a woman with BSS who was closely monitored throughout pregnancy and postpartum period, and had a judiciously planned birth. Conclusion: Management of BSS during pregnancy is still unclear. However, it is important to strictly control platelet counts and plan the birth in advance.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofOpen Journal of Obstetrics and Gynecology. Irvine. Vol. 9, no. 6 (May 2019), p. 838-844pt_BR
dc.rightsOpen Accessen
dc.subjectMulherespt_BR
dc.subjectBernard-Soulieren
dc.subjectGravidezpt_BR
dc.subjectHemostasisen
dc.subjectThrombocytopeniaen
dc.subjectSíndrome de Bernard-Soulierpt_BR
dc.subjectPregnancyen
dc.subjectTrombocitopeniapt_BR
dc.subjectObstetricsen
dc.subjectHemostasept_BR
dc.subjectPostpartum hemorrhageen
dc.titleBernard-Soulier syndrome in pregnancy : a case reportpt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001123142pt_BR
dc.type.originEstrangeiropt_BR


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