[Kartagener sindrome (primary ciliary dyskinesia). Report of a case and literature review].

V Pino Rivero, G Pardo Romero, R J Iglesias González, M Rodríguez Carmona, F del Castillo Beneyto
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Abstract

Kartagener syndrome (a clinical variant of primary ciliary dyskinesia) is a recessive autossomical disease characterized by the triad of chronic sinusitis, bronchiectasis and situs inversus with dextrocardia. We report one case described in a 8 years old boy who besides presented a seromucous otitis and bronchitis of repetition. Finally we performed a short bibliographic review at respect of this uncommon pathology.

Kartagener综合征(原发性纤毛运动障碍)。病例报告及文献综述]。
Kartagener综合征(原发性纤毛运动障碍的一种临床变异)是一种隐性常染色体疾病,以慢性鼻窦炎、支气管扩张和心右位倒置为特征。我们报告了一例8岁男孩的病例,他除了表现为浆液性中耳炎和重复性支气管炎之外。最后,我们对这种罕见的病理进行了简短的文献回顾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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