Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/43653
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dc.contributor.authorMartínez-Quintana, Efrénen_US
dc.contributor.authorRodríguez-González, Faynaen_US
dc.contributor.authorGopar-Gopar, Silviaen_US
dc.date.accessioned2018-11-21T16:50:12Z-
dc.date.available2018-11-21T16:50:12Z-
dc.date.issued2016en_US
dc.identifier.issn1061-1711en_US
dc.identifier.urihttp://hdl.handle.net/10553/43653-
dc.description.abstractHereditary hemorrhagic telangiectasia, also known as Osler–Weber–Rendu syndrome, is an autosomal dominant genetic disorder that leads to epistaxis, gastrointestinal bleeding, iron deficiency anemia, and arteriovenous malformations at the lungs, the liver, and the brain. However, due to its rarity and its unspecific findings on routine examinations, diagnosis is not easy unless suspected due to hypoxemia or paradoxical embolism. We present a case of a 46-year-old-woman with hereditary hemorrhagic telangiectasia and hypoxemia who presented a myocardial infarction secondary to paradoxical embolism through pulmonary arteriovenous malformations.en_US
dc.languageengen_US
dc.publisher1061-1711-
dc.relation.ispartofInternational Journal of Angiologyen_US
dc.sourceInternational Journal of Angiology [ISSN 1061-1711], v. 25, p. e81-e83en_US
dc.subject320501 Cardiologíaen_US
dc.subject.otherHereditary hemorrhagic teangiectasien_US
dc.subject.otherOsler–Weber–Rendu syndromeen_US
dc.subject.otherPulmonary arteriovenous malformationsen_US
dc.subject.otherMyocardial infarctionen_US
dc.titleHereditary Hemorrhagic Telangiectasia and Myocardial Infarctionen_US
dc.typeinfo:eu-repo/semantics/articlees
dc.typeArticlees
dc.identifier.doi10.1055/s-0035-1551795en_US
dc.identifier.scopus84929698731-
dc.contributor.authorscopusid23485891800-
dc.contributor.authorscopusid24825586600-
dc.contributor.authorscopusid56091587800-
dc.description.lastpagee83-
dc.description.firstpagee81-
dc.relation.volume25-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.ulpgces
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.fullNameMartínez Quintana, Efrén-
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