关键词: 原发性纤毛运动障碍, 计算机断层摄影术, Kartagener综合征

Abstract:

Objective: To explore the clinical features of the patients with Kartagener syndrome(KS), and to review the associated literaturesabout its diagnosis and treatment, and to improve the understanding of the clinician for KS.Methods: The clinical data of one KS patient was collected and the therapeutic effect was analyzed.Results: The patient was clearly diagnoed as KS after relevant examinations.The symptoms such as cough,expectoration,and shortness of breath of the patient were improved after symptomatic treatment,such as anti-inflammation,relieving cough and reducing sputum,and spasmolysis.Conclusion: KS is a congenital autosomal recessive disease.The clinical treatment can only relieve the symptoms,but the structural change is irreversible.The genetics of KS needs further study to reduce its occurrence.

Key words: primary ciliary dyskinesia, Kartagener syndrome, computerized tomography