A case of Kartagener’s syndrome: Importance of early diagnosis and treatment

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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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Detalles Bibliográficos
Autores principales: Gupta, Sanjay, Handa, Kumud K., Kasliwal, Ravi R., Bajpai, Pankaj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3758738/
https://www.ncbi.nlm.nih.gov/pubmed/24019633
http://dx.doi.org/10.4103/0971-6866.116107

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3758738/
https://www.ncbi.nlm.nih.gov/pubmed/24019633
http://dx.doi.org/10.4103/0971-6866.116107

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