Literature DB >> 16627448

Phenotype reveals genotype in a Greek long QT syndrome family.

Aris Anastasakis1, Christina-Maria Kotta, Stavros Kyriakogonas, Bernd Wollnik, Artemisia Theopistou, Christodoulos Stefanadis.   

Abstract

We aimed to verify the long 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.

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Year:  2006        PMID: 16627448     DOI: 10.1093/europace/eul012

Source DB:  PubMed          Journal:  Europace        ISSN: 1099-5129            Impact factor:   5.214


  3 in total

1.  Enhanced effects of isoflurane on the long QT syndrome 1-associated A341V mutant.

Authors:  Ikuomi Mikuni; Carlos G Torres; Tania Bakshi; Akihito Tampo; Brian E Carlson; Martin W Bienengraeber; Wai-Meng Kwok
Journal:  Anesthesiology       Date:  2015-04       Impact factor: 7.892

2.  Partial restoration of the long QT syndrome associated KCNQ1 A341V mutant by the KCNE1 β-subunit.

Authors:  Ikuomi Mikuni; Carlos G Torres; Martin W Bienengraeber; Wai-Meng Kwok
Journal:  Biochim Biophys Acta       Date:  2011-08-10

3.  Cardiac ion channel gene mutations in Greek long QT syndrome patients.

Authors:  C-M Kotta; A Anastasakis; K Gatzoulis; J Papagiannis; P Geleris; C Stefanadis
Journal:  J Appl Genet       Date:  2010       Impact factor: 2.653

  3 in total

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