摘要
卡塔格内综合征(Kartagener syndrome,KS)是一种常染色体隐性遗传病,有家族遗传倾向,是原发性纤毛运动障碍(primary ciliary dyskinesia,PCD)的一个特殊类型,其主要临床特征为支气管扩张、内脏转位和慢性鼻窦炎,患者常在幼年时就表现出相应的临床症状。本文回顾性分析微山县人民医院内分泌科收治的1例KS患者的临床特征,并进行文献复习。
Kartagener syndrome(KS)is an autosomal recessive inherited disease with a familial genetic tendency.It is a special type of primary ciliary dyskinesia(PCD),characterized by bronchiectasis,visceral translocation,and chronic sinusitis,patients often exhibit corresponding clinical symptoms at an early age.This article retrospectively analyzes the clinical data of a patient with KS admitted to our department,and reviews the literature on this disease.
作者
李中川
庞娟娟
华纯山
李丽萍
吴家云
唐巧真
李小娥
LI Zhongchuan;PANG Juanjuan;HUA Chunshan;LI Liping;WU Jiayun;TANG Qiaozhen;LI Xiao'e(Department of Endocrinology,Weishan People's Hospital,Jining,Shandong,277600,China)
出处
《当代医学》
2025年第4期149-153,共5页
Contemporary Medicine
