| Literature DB >> 25273952 |
Mikael Hanninen1, George J Klein, Zachary Laksman, Susan S Conacher, Allan C Skanes, Raymond Yee, Lorne J Gula, Peter Leong-Sit, Jaimie Manlucu, Andrew D Krahn.
Abstract
The acceptance and yield of family screening in genotype-negative long QT syndrome (LQTS) remains incompletely characterized. In this study of family screening for phenotype-definite Long QT Syndrome (LQTS, Schwartz score ≥3.5), probands at a regional Inherited Cardiac Arrhythmia clinic were reviewed. All LQTS patients were offered education by a qualified genetic counselor, along with materials for family screening including electronic and paper correspondence to provide to family members. Thirty-eight qualifying probands were identified and 20 of these had family members who participated in cascade screening. The acceptance of screening was found to be lower among families without a known pathogenic mutation (33 vs. 77 %, p = 0.02). A total of 52 relatives were screened; fewer relatives were screened per index case when the proband was genotype-negative (1.7 vs. 3.1, p = 0.02). The clinical yield of screening appeared to be similar irrespective of gene testing results (38 vs. 33 %, p = 0.69). Additional efforts to promote family screening among gene-negative long QT families may be warranted.Entities:
Mesh:
Year: 2014 PMID: 25273952 DOI: 10.1007/s10897-014-9776-6
Source DB: PubMed Journal: J Genet Couns ISSN: 1059-7700 Impact factor: 2.537