Caballero iglesias r, sanchez lopez f, alcazar iribarren m. Approximately 50% of patient with primary ciliary dyskinesia. Temas actualidad 1bianca ethel gutierrezamavizca, 2 sindrome. It is a genetic condition with an autosomal recessive inheritance,1,2 comprising a triad of situs inversus, bronchiectasis and sinusitis. 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. Url consultato il 9 dicembre 2007 archiviato dall url originale il 6 agosto 2007. Kartagener s syndrome ks is a subset of a larger group of ciliary motility disorders called primary ciliary dyskinesias pcds. Longitudinal lung function and structural changes in children with primary ciliary dyskinesia. An unusual regression of the symptoms of kartageners syndrome. Leigh mw, pittman je, carson jl, ferkol tw, dell sd, davis sd, et al. Pdf kartageners syndrome ks is an autosomal recessive subgroup of primary ciliary dyskinesia pcd. Mar 20, 2020 kartagener syndrome, current data on a classical disease.
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