Kartagener’S Syndrome

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

  • SEVİL ARI YUCA: VAN 100. YIL ÜNİVERSİTESİ
  • KÖKSAL YUCA: SELÇUK ÜNİVERSİTESİ
  • BERFİN ÖZGÖKÇE: VAN 100. YIL ÜNİVERSİTESİ
  • CAHİDE YILMAZ: MUSTAFA KEMAL ÜNİVERSİTESİ
  • SERHAT AVCU: VAN 100. YIL ÜNİVERSİTESİ
  • 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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Conflict of interest : Yok
This article is published under the CC BY-NC 4.0 license.
Selcuk Medical Journal
2011, Vol. 27 (1)
ISSN: 1017-6616
E-ISSN: 2149-8059
Received : , Accepted : , Published Online :