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Kartagener syndrome: A case report
Kartagener syndrome is a rare, autosomal recessive genetic disorder that causes defects in the action of ciliary movement, comprises of triad situs inversus, chronic sinusitis, and bronchiectasis. We present the case of a 3-year-old boy with repeated respiratory infections and pneumonic infections p...
Autores principales: | Ibrahim, Rahaf, Daood, Huda |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Canadian Society of Respiratory Therapists
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8059757/ https://www.ncbi.nlm.nih.gov/pubmed/33912655 http://dx.doi.org/10.29390/cjrt-2020-064 |
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