Genetics and pulmonary hypertension

被引:7
|
作者
Loyd, JE [1 ]
机构
[1] Vanderbilt Med Ctr N, Dept Pulm & Crit Care Med, Nashville, TN 37232 USA
关键词
cell surface receptors; epidemiology; genetics; germline mutation; hemodynamics; linkage; protein-serine-threonine kinases; pulmonary hypertension;
D O I
10.1378/chest.122.6_suppl.284S
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Primary pulmonary hypertension (PPH) is a serious pulmonary vascular disease occurring mostly in adult women. Although its occurrence in families was reported within a few years after the original clinical report, PPH was formerly believed rarely to have a genetic basis. Recent progress has not only clarified a basic molecular mechanism for PPH in families, but has also identified mutations of the same gene in many sporadic PPH patients, suggesting that its basis is commonly genetic. Extensive investigations in many centers are now in progress to provide a complete dissection of all the pathogenetic mechanisms of PPH.
引用
收藏
页码:284S / 286S
页数:3
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