Articles on Kartagener’s syndrome

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

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...