[卡塔格内综合征（原发性纤毛运动障碍）。1例报告及文献复习]

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

作者信息

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

机构信息

Hospital Campo Arañuelo, Navalmoral de la Mata, Cáceres.

出版信息

An Otorrinolaringol Ibero Am. 2007;34(3):251-6.

PMID:17725169

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.

摘要

卡塔格内综合征（原发性纤毛运动障碍的一种临床变异型）是一种隐性常染色体疾病，其特征为慢性鼻窦炎、支气管扩张和内脏转位伴右位心三联征。我们报告一例8岁男孩的病例，该男孩除了患有浆液性中耳炎和复发性支气管炎外，还患有上述病症。最后，我们针对这种罕见病症进行了简短的文献综述。