Genetic Causes of Bronchiectasis

被引:8
|
作者
Gould, Christine M. [1 ,2 ]
Freeman, Alexandra F. [3 ]
Olivier, Kenneth N. [3 ]
机构
[1] Childrens Natl Med Ctr, Div Pulm & Sleep Med, Washington, DC 20010 USA
[2] Walter Reed Natl Mil Med Ctr, Dept Pediat, Bethesda, MD 20889 USA
[3] NIAID, Lab Clin Infect Dis, NIH, Bethesda, MD 20892 USA
关键词
Bronchiectasis; Genetic; Impaired mucociliary clearance; Immunodeficiency; Congenital anomalies of the airway; PRIMARY CILIARY DYSKINESIA; YELLOW-NAIL-SYNDROME; MIDDLE LOBE SYNDROME; COMMON VARIABLE IMMUNODEFICIENCY; MOUNIER-KUHN-SYNDROME; X-LINKED AGAMMAGLOBULINEMIA; WILLIAMS-CAMPBELL-SYNDROME; FAMILIAL CONGENITAL BRONCHIECTASIS; RESOLUTION COMPUTED-TOMOGRAPHY; DYNEIN ARM DEFECTS;
D O I
10.1016/j.ccm.2012.03.002
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Our understanding of the pathologic cycle leading to the development of bronchiectasis is enhanced by greater understanding of the genetic influences contributing to its development. Genome-wide linkage analysis, family-based genetic linkage studies, and the testing of candidate genes have all greatly advanced our understanding of the complexity of the genetic basis of bronchiectasis. This article discusses how allelic variations, gene modifiers, HLA associations, and the interplay of developmental, host, and environmental factors all contribute in lesser and greater degrees, depending on the specific disease, toward the development of bronchiectasis in a spectrum of disease processes.
引用
收藏
页码:249 / +
页数:16
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