Genetic Testing for Cardiomyopathies in Clinical Practice

被引:14
|
作者
Ingles, Jodie [1 ,2 ,3 ]
Bagnall, Richard D. [1 ,2 ]
Semsarian, Christopher [1 ,2 ,3 ]
机构
[1] Centenary Inst, Agnes Ginges Ctr Mol Cardiol, Sydney, NSW, Australia
[2] Univ Sydney, Sydney Med Sch, Sydney, NSW, Australia
[3] Royal Prince Alfred Hosp, Dept Cardiol, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
Hypertrophic cardiomyopathy; Dilated cardiomyopathy; Arrhythmogenic right ventricular cardiomyopathy; Genetic testing; Genetic counseling; SUDDEN CARDIAC DEATH; INHERITED CARDIOVASCULAR-DISEASES; COST-EFFECTIVENESS MODEL; HYPERTROPHIC CARDIOMYOPATHY; DILATED CARDIOMYOPATHY; UNRELATED PATIENTS; NOONAN SYNDROME; DANON DISEASE; YOUNG-ADULTS; VARIANTS;
D O I
10.1016/j.hfc.2017.12.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiac genetic testing for inherited cardiomyopathies has become a routine aspect of care. Advances in genetic testing technologies have made testing more comprehensive and affordable. With this increase comes greater understanding of the genetic basis of these diseases, but also shines a light on the challenges. Ability to ascertain whether a rare variant is causative of disease is problematic. A genetic diagnosis in a family can offer an invaluable tool for cascade genetic testing of at-risk relatives and avenues for reproductive testing options. A careful approach to cardiac genetic testing that recognizes where there is potential for harm ensures the best possible outcomes for families.
引用
收藏
页码:129 / 137
页数:9
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