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Article Number - BBBD259509


Vol.2(2), pp. 15-18 , February 2011

ISSN: 2141-6532


Review

Kartagener’s syndrome- A case report



Jayita Poduval
  • Jayita Poduval
  • Department of Otolaryngology, Faculty of Medicine, AIMST University Semeling, Bedong-08100, Malaysia.
  • Google Scholar
Murali Poduval
  • Murali Poduval
  • Faculty of Medicine, AIMST University, Malaysia.
  • Google Scholar







 Accepted: 10 February 2011  Published: 28 February 2011

Copyright © 2011 Author(s) retain the copyright of this article.
This article is published under the terms of the Creative Commons Attribution License 4.0


 

Primary Ciliary Dyskinesia (PCD) is a genetic disorder with an autosomal recessive mode of inheritance.It is caused by a defect in the structure of cilia, due to which ciliary movement, and consequently, its function, are impaired.  Sinusitis, nasal polyposis, and otitis media with effusion are commonly seen among patients presenting to the otolaryngologist, and PCD should be considered as an aetiological factor in these cases, especially in the refractory ones. A case presenting to an otolaryngologist is described with a review of salient literature.

 

Key words: Nasal polyp, primary ciliary dyskinesia, Kartagener's syndrome.

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APA (2011). Kartagener’s syndrome- A case report. Medical Case Studies, 2(2), 15-18.
Chicago Jayita Poduval and Murali Poduval. "Kartagener’s syndrome- A case report." Medical Case Studies 2, no. 2 (2011): 15-18.
MLA Jayita Poduval and Murali Poduval. "Kartagener’s syndrome- A case report." Medical Case Studies 2.2 (2011): 15-18.
   
DOI
URL http://academicjournals.org/journal/MCS/article-abstract/BBBD259509

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