Inherited diseases and syndromes leading to aortic aneurysms and dissections

被引:43
作者
Caglayan, Ahmet Okay [1 ]
Dundar, Munis [2 ]
机构
[1] Kayseri Educ & Res Hosp, Dept Med Genet, TR-38010 Kayseri, Turkey
[2] Erciyes Univ, Fac Med, Dept Med Genet, Kayseri, Turkey
关键词
Aneurysms; Dissections; Genetics; EHLERS-DANLOS-SYNDROME; PATENT DUCTUS-ARTERIOSUS; SYNDROME TYPE-IV; CONGENITAL HEART-DISEASE; EGF-LIKE DOMAIN; MARFAN-SYNDROME; TURNER-SYNDROME; CARDIOVASCULAR MALFORMATIONS; MATRIX METALLOPROTEINASES; GENOMIC ORGANIZATION;
D O I
10.1016/j.ejcts.2009.01.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genes affect virtually all human characteristics and diseases. These influences can be ascertained in individual patients through a review of the family history physical examination and the use of medical diagnostics. Aneurysms and dissections are a leading cause of morbidity and mortality, in addition to medical expense, and, on the whole, their specific molecular mechanisms are beginning to be identified. Over the past decade, genetic tests have become available for numerous heritable disorders especially inherited with mendelian models. An important fact is that the results of genetic tests may also be useful beyond the individual affected by the genetic disorder. Depending upon the disorder, knowledge of carrier status may be important. Because of these facts, some essential information regarding basic genetics of aneurysm and dissection has been presented in this study. (C) 2009 European Association for Cardio-Thoracic Surgery. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:931 / 940
页数:10
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