Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline

被引：325

作者：

Hershberger, Ray E. ^{[1
]}

Lindenfeld, Joann ^{[2
]}

Mestroni, Luisa ^{[2
,3
]}

Seidman, Christine E. ^{[4
,5
]}

Taylor, Matthew R. G. ^{[2
,3
]}

Towbin, Jeffrey A. ^{[6
]}

机构：

[1] Univ Miami, Sch Med, Div Cardiovasc, Miami, FL 33101 USA

[2] Univ Colorado, Hlth Sci Ctr, Div Cardiol, Denver, CO 80262 USA

[3] Univ Colorado, Hlth Sci Ctr, Adult Med Genet Program, Denver, CO 80262 USA

[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA

[5] Harvard Univ, Brigham & Womens Hosp, Sch Med, Cardiovasc Genet Ctr, Boston, MA 02115 USA

[6] Baylor Coll Med, Div Pediat Cardiol, Houston, TX 77030 USA

来源：

JOURNAL OF CARDIAC FAILURE | 2009年 / 15卷 / 02期

关键词：

RIGHT-VENTRICULAR CARDIOMYOPATHY; LAMIN-A/C GENE; MYOSIN HEAVY-CHAIN; CARDIAC TROPONIN-I; FAMILIAL HYPERTROPHIC CARDIOMYOPATHY; X-LINKED GENE; DILATED CARDIOMYOPATHY; CONDUCTION-SYSTEM; ACTIN GENE; MUTATIONAL ANALYSIS;

D O I：

10.1016/j.cardfail.2009.01.006

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Substantial progress has been made recently in understanding the genetic basis of cardiomyopathy. Cardiomyopathies with known genetic cause include hypertrophic (HCM), dilated (DCM), restrictive (RCM), arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and left ventricular noncompaction (LVNC). HCM, DCM, and RCM have been recognized as distinct clinical entities for decades, whereas ARVD/C and LVNC are relative newcomers to the field. Hence the clinical and genetic knowledge for each cardiomyopathy varies, as do the recommendations and strength of evidence. (J Cardiac Fail 2009;15:83-97)

引用

页码：83 / 97

页数：15

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