PDF(Pubmed)
Abstract：
Kartagener syndrome (KS), also known as primary ciliary dyskinesia, is a rare genetic disorder commonly diagnosed early in childhood. It is characterized by a triad of findings, namely, situs inversus, chronic sinusitis, and bronchiectasis. Here, we present the case of a 73-year-old female who incidentally presented the KS triad during her imaging tests in the emergency department of our institution for COVID-19 symptoms.
摘要：
Kartagener综合征（KS），也称为原发性纤毛运动障碍，是一种罕见的遗传性疾病，通常在儿童早期被诊断出来。它的特点是三位一体的发现，即,situsinversus,慢性鼻窦炎,还有支气管扩张.这里,我们介绍了一例73岁的女性,她在我院急诊科进行的COVID-19症状影像学检查中偶然出现KS三联征.
