医学
卡塔格综合征
寿命
儿科
支气管扩张
粘液纤毛清除率
原发性睫状体运动障碍
内科学
老年学
肺
作者
Richard Miller,Matthew B. Divertie
出处
期刊:Chest
[Elsevier]
日期:1972-08-01
卷期号:62 (2): 130-135
被引量:65
标识
DOI:10.1378/chest.62.2.130
摘要
Clinical observations of 19 patients with Kartagener's syndrome seen during the past 25 years support the concept of congenital functional or anatomic defects in the mucociliary epithelium and its supporting structures. The case of a woman with this syndrome, who is alive at the age of 72 years, is detailed to suggest that, with reasonable medical supervision, the syndrome is compatible with a full life span. Clinical observations of 19 patients with Kartagener's syndrome seen during the past 25 years support the concept of congenital functional or anatomic defects in the mucociliary epithelium and its supporting structures. The case of a woman with this syndrome, who is alive at the age of 72 years, is detailed to suggest that, with reasonable medical supervision, the syndrome is compatible with a full life span.
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