Genetic testing in cardiovascular diseases

被引:5
|
作者
Hofman, Nynke [2 ]
van Langen, Irene [2 ]
Wilde, Arthur A. M. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Cardiol, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Clin Genet, NL-1105 AZ Amsterdam, Netherlands
关键词
cardiogenetics; genetic counseling; genetic testing; LONG-QT SYNDROME; POLYMORPHIC VENTRICULAR-TACHYCARDIA; CARDIOMYOPATHY MUTATION CARRIERS; QUALITY-OF-LIFE; HYPERTROPHIC CARDIOMYOPATHY; SPECTRUM; YIELD; PHENOTYPE; DIAGNOSIS; FAMILY;
D O I
10.1097/HCO.0b013e3283374d69
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review To review the current state and different aspects, including the yield, of genetic counseling and genetic testing in inherited heart disease. Recent findings The number of counselees is growing rapidly all over the world, and the first studies about patients' perspectives and follow-up have been published. Progress has been made by gene-specific studies on long QT syndrome to judge the relevance of detected mutations in the specific domains. Summary With the increasing identification of associated genes and available techniques in molecular testing of the inherited heart diseases, the diagnostic yield of mutation analysis is growing rapidly. To determine the relevance of all these mutations, ongoing research is needed. Furthermore, the process of genetic counseling can be optimized and extended with cascade screening, which leads to identifying patients at risk and timely treatment.
引用
收藏
页码:243 / 248
页数:6
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