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dc.contributor.authorGutiérrez Zuñiga, Daniela
dc.contributor.authorSolarte Bothe, Daniel
dc.contributor.authorCelis Preciado, Carlos Andrés
dc.date.accessioned2022-05-31T15:34:06Z
dc.date.accessioned2023-05-11T17:18:12Z
dc.date.available2022-05-31T15:34:06Z
dc.date.available2023-05-11T17:18:12Z
dc.date.created2017
dc.identifierhttps://revistas.javeriana.edu.co/index.php/vnimedica/article/view/19800
dc.identifier.issn0041-9095
dc.identifier.urihttps://hdl.handle.net/20.500.12032/106566
dc.description.abstractKartagener syndrome us a rare autosomal recessive disease (one in every 32,000 births), characterized by a triad of bronchiectasis, chronic sinusitis and situs inversus. We present the case of a 24-year-old male with this disease and we review the pathoph
dc.formatPDFspa
dc.format.mimetypeapplication/pdfspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subjectKartagener Syndrome
dc.subjectPrimary Ciliary Dyskinesia
dc.subjectSitus Inversus
dc.titleKartagener syndrome : case report and literature review


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