Phenotype reveals genotype in a Greek long QT syndrome family

被引:5
|
作者
Anastasakis, Aris
Kotta, Christina-Maria
Kyriakogonas, Stavros
Wollnik, Bernd
Theopistou, Artemisia
Stefanadis, Christodoulos
机构
[1] Univ Athens, Dept Cardiol 1, Sch Med, Div Inherited Cardiovasc Dis, GR-11528 Athens, Greece
[2] Istanbul Univ, Inst Child Hlth, Dept Med Genet, Istanbul, Turkey
来源
EUROPACE | 2006年 / 8卷 / 04期
关键词
long QT syndrome; syncope; genotype; phenotype;
D O I
10.1093/europace/eul012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We aimed to verify the tong QT syndrome (LQTS) genotype in a family with strong evidence of LQTS type 1 (LQT1) on the basis of so far established genotype-phenotype correlations. Genetic testing for mutations in the KCNQ1 potassium channel gene revealed an A341V mutation in three generations of the family. Existing genotype-phenotype correlations were correctly predictive of the genotype in the case of this family, despite the fact that there are no previously reported data for the Greek LQTS genetic pool. Thus, genotype-phenotype correlations are often a helpful tool in the management of LQTS patients and their families.
引用
收藏
页码:241 / 244
页数:4
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