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A case of Kartagener’s syndrome: Importance of early diagnosis and treatment
Kartagener’s syndrome is a very rare congenital malformation comprising of a classic triad of sinusitis, situs inversus and bronchiectasis. Primary ciliary dyskinesia is a genetic disorder with manifestations present from early life and this distinguishes it from acquired mucociliary disorders. Appr...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3758738/ https://ncbi.nlm.nih.gov/pubmed/24019633 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.116107 |
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