Kartagener综合征(原发性纤毛运动障碍)。病例报告及文献综述]。

Anales otorrinolaringologicos ibero-americanos Pub Date : 2007-01-01

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

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引用次数: 0

摘要

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。

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

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.

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Anales otorrinolaringologicos ibero-americanos

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