Kartagener syndrome : case report and literature review
Kartagener 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
- Autores:
-
Gutiérrez Zuñiga, Daniela
Solarte Bothe, Daniel
Celis Preciado, Carlos Andrés
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2017
- Institución:
- Pontificia Universidad Javeriana
- Repositorio:
- Repositorio Universidad Javeriana
- Idioma:
- OAI Identifier:
- oai:repository.javeriana.edu.co:10554/59907
- Acceso en línea:
- https://revistas.javeriana.edu.co/index.php/vnimedica/article/view/19800
http://hdl.handle.net/10554/59907
https://doi.org/10.11144/Javeriana.umed58-1.kart
- Palabra clave:
- Kartagener Syndrome
Primary Ciliary Dyskinesia
Situs Inversus
- Rights
- License
- Atribución-NoComercial 4.0 Internacional