Nsindrome de kartagener pdf

The mechanism of the reversal of laterality remains an enigma, but it appears to be strictly an abolition. Approximately 50% of patient with primary ciliary dyskinesia. Learn about its symptoms and how its diagnosed and treated. The kartagener syndrome is a rare recessive autossomical. Chest xrays or computed tomography ct scans can detect lung changes characteristic of the syndrome. Kartagener syndrome is a subset of primary ciliary dyskinesia, an autosomal recessive condition characterized by an abnormal ciliary structure or function, leading to impaired mucociliary clearance. An autosomal recessive disorder characterized by a triad of dextrocardia. Kartagener syndrome is recognized by the three main symptoms of chronic sinusitis, bronchiectasis and situs inversus.