Genetic counselling and testing in adults with congenital heart disease: A consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Human Genetics

被引:35
|
作者
De Backer, Julie [1 ,2 ,3 ]
Bondue, Antoine [4 ]
Budts, Werner [5 ,6 ]
Evangelista, Arturo [3 ,7 ]
Gallego, Pastora [8 ]
Jondeau, Guillaume [3 ,9 ]
Loeys, Bart [3 ,10 ,11 ,12 ]
Pena, Maria L. [8 ]
Teixido-Tura, Gisela [3 ,7 ]
van de Laar, Ingrid [3 ,13 ]
Verstraeten, Aline [10 ,11 ,12 ]
Hesselink, Jolien Roos [3 ,14 ]
机构
[1] Ghent Univ Hosp, Dept Cardiol, C Heymanslaan 10, B-9000 Ghent, Belgium
[2] Ghent Univ Hosp, Ctr Med Genet, C Heymanslaan 10, B-9000 Ghent, Belgium
[3] European Reference Network Rare Multisyst Vasc Di, HTAD Rare Dis Working Grp, Paris, France
[4] Univ Libre Bruxelles, Dept Cardiol, Brussels, Belgium
[5] Univ Hosp Leuven, Congenital & Struct Cardiol, Leuven, Belgium
[6] Katholieke Univ Leuven, Dept Cardiovasc Sci, Leuven, Belgium
[7] Hosp Univ Vall dHebron, Serv Cardiol, VHIR CIBER CV, Barcelona, Spain
[8] Hosp Univ Virgen del Rocio, Dept Cardiol, Seville, Spain
[9] Hop Bichat Claude Bernard, Ctr Natl Maladie Rare Syndrome Marfan & Apparente, Paris, France
[10] Univ Antwerp, Ctr Med Genet, Antwerp, Belgium
[11] Antwerp Univ Hosp, Antwerp, Belgium
[12] Radboud Univ Nijmegen, Dept Human Genet, Med Ctr, Nijmegen, Netherlands
[13] Erasmus MC, Dept Clin Genet, Rotterdam, Netherlands
[14] Erasmus MC, Dept Cardiol, Rotterdam, Netherlands
关键词
Genetic testing; genetic counseling; adult congenital heart disease; heritable thoracic aortic disease; 22Q11.2 DELETION SYNDROME; DE-NOVO MUTATIONS; CARDIAC DEFECTS; HUMAN JAGGED1; TETRALOGY; STATEMENT; RECURRENCE; MICROARRAY; VARIANTS; NKX2-5;
D O I
10.1177/2047487319854552
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Thanks to a better knowledge of the genetic causes of many diseases and an improvement in genetic testing techniques, genetics has gained an important role in the multidisciplinary approach to diagnosis and management of congenital heart disease and aortic pathology. With the introduction of strategies for precision medicine, it is expected that this will only increase further in the future. Because basic knowledge of the indications, the opportunities as well as the limitations of genetic testing is essential for correct application in clinical practice, this consensus document aims to give guidance to care-providers involved in the follow-up of adults with congenital heart defects and/or with hereditary aortic disease. This paper is the result of a collaboration between the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Human Genetics. Throughout the document, the importance of correct counseling in the process of genetic testing is emphasized, indications and timing for genetic studies are discussed as well as the technical modalities of genetic testing. Finally, the most important genetic diseases in adult congenital heart disease and aortic pathology are also discussed.
引用
收藏
页码:1423 / 1435
页数:13
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