吉林大学学报（医学版）2016，Vol.42Issue(6)：1194-1196,3.DOI:10.13481/j.1671-587x.20160628
Kartagener综合征1例报告并文献复习
Kartagener syndrome:A case report and literature review
摘要
Abstract
Objective:To explore the clinical features of the patients with Kartagener syndrome (KS),and to review the associated literatures about 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.关键词
Kartagener综合征/原发性纤毛运动障碍/计算机断层摄影术Key words
Kartagener syndrome/primary ciliary dyskinesia/computerized tomography分类
医药卫生引用本文复制引用
张辉,刘颖,张艳霞,张连莲,孙璐瑶,于振香..Kartagener综合征1例报告并文献复习[J].吉林大学学报（医学版）,2016,42(6):1194-1196,3.基金项目
吉林省科技厅科研基金资助课题 （）
