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Sickle cell disease: A diagnosis to keep in mind

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dc.creatorZúñiga C, Pamelaspa
dc.creatorMartínez G, Cindyspa
dc.creatorGonzález R, Lina Mspa
dc.creatorRendón C, Diana Sspa
dc.creatorRojas R, Nicolásspa
dc.creatorBarriga C, Franciscospa
dc.creatorWietstruck P, María Angélicaspa
dc.date.accessioned2020-05-25T23:59:00Z
dc.date.available2020-05-25T23:59:00Z
dc.date.created2018spa
dc.description.abstractSickle cell disease (SCD) is an autosomal recessive genetic disorder. It is the most frequent structural hemoglobinopathy worldwide, and it is produced by an alteration in the globin chain genes. In Chile, there is no data on the prevalence of SCD since it is considered a very rare condition. The incidence of this disease has been increasing due to migration of people from areas with greater presence of SCD. It is important to know and consider this diagnosis in a selected group of patients with anemia, in order to prevent and treat the different complications of this disease. This article reviews the most recent information that shows new concepts in the knowledge of the physiopathology, and especially publications of guidelines and consensus in relation to the diagnosis and management of this condition. © 2018, Sociedad Chilena de Pediatria. All rights reserved.eng
dc.format.mimetypeapplication/pdf
dc.identifier.doihttps://doi.org/10.4067/S0370-41062018005000604
dc.identifier.issn07176228
dc.identifier.issn03704106
dc.identifier.urihttps://repository.urosario.edu.co/handle/10336/22967
dc.language.isoengspa
dc.publisherSociedad Chilena de Pediatriaspa
dc.relation.citationEndPage529
dc.relation.citationIssueNo. 4
dc.relation.citationStartPage525
dc.relation.citationTitleRevista Chilena de Pediatria
dc.relation.citationVolumeVol. 89
dc.relation.ispartofRevista Chilena de Pediatria, ISSN:07176228, 03704106, Vol.89, No.4 (2018); pp. 525-529spa
dc.relation.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85053086268&doi=10.4067%2fS0370-41062018005000604&partnerID=40&md5=8b0c0a3dd5547de3ef3d18b1c19d7fc1spa
dc.rights.accesRightsinfo:eu-repo/semantics/openAccess
dc.rights.accesoAbierto (Texto Completo)spa
dc.source.instnameinstname:Universidad del Rosariospa
dc.source.reponamereponame:Repositorio Institucional EdocURspa
dc.subject.keywordAnemiaspa
dc.subject.keywordHemoglobinopathyspa
dc.subject.keywordMorbidityspa
dc.subject.keywordPathophysiologyspa
dc.subject.keywordPrevalencespa
dc.subject.keywordReviewspa
dc.subject.keywordSickle cell anemiaspa
dc.subject.keywordDifferential diagnosisspa
dc.subject.keywordHumanspa
dc.subject.keywordMultimodality cancer therapyspa
dc.subject.keywordPrognosisspa
dc.subject.keywordSickle cell anemiaspa
dc.subject.keywordAnemiaeng
dc.subject.keywordCombined modality therapyspa
dc.subject.keywordDiagnosiseng
dc.subject.keywordHumansspa
dc.subject.keywordPrognosisspa
dc.subject.keywordAnemiaspa
dc.subject.keywordHemoglobinspa
dc.subject.keywordHemoglobinopathiesspa
dc.subject.keywordSickle cellspa
dc.titleSickle cell disease: A diagnosis to keep in mindspa
dc.title.TranslatedTitleEnfermedad de células falciformes: Un diagnóstico para tener presentespa
dc.typearticleeng
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersion
dc.type.spaArtículospa
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