Kartagener’S Syndrome

SEVİL ARI YUCA, KÖKSAL YUCA, BERFİN ÖZGÖKÇE, CAHİDE YILMAZ, SERHAT AVCU

  • Year : 2011
  • Vol : 27
  • Issue : 1
  •  Page : 34-36
Primary ciliary dyskinesia is an autosomal recessive, with abnormalities in ciliary structure and function in an outgoing and 20,000 live birth, is a rare disease. Kartagener’s syndrome is characterized by the combination of primary ciliary dyskinesia and situs inversus, and occurs in approximately half of patients with ciliary dyskinesia. It presented here a 12-year-old male patient had a history of recurrent respiratory tract infections and pneumonia.
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Description : None of the authors, any product mentioned in this article, does not have a material interest in the device or drug. Research, not supported by any external organization. grant full access to the primary data and, if requested by the magazine they agree to allow the examination of data.
Kartagener’S Syndrome
, Vol. 27 (1)
Received : 23.04.2010, Accepted : 23.04.2010, Published Online : 13.08.2018
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ISSN:1017-6616;
E-ISSN:2149-8059;