| Literature DB >> 25041374 |
J M Lopez-Ayala1, M Ortiz-Genga2, I Gomez-Milanes3, D Lopez-Cuenca1, F Ruiz-Espejo3, J J Sanchez-Munoz1, M J Oliva-Sandoval1, L Monserrat2, J R Gimeno1.
Abstract
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an important cause of malignant arrhythmia and sudden death particularly in young people. Although it is considered a desmosomal disease, mutations in non-desmosomal genes have also been identified. We report on a family where a mutation in LDB3 is associated with this condition. The index case and first and second degree relatives underwent a complete clinical evaluation: physical examination, electrocardiography (ECG), signal-averaged ECG, 2D echocardiogram, cardiac magnetic resonance and 24-h monitoring. After ruling out mutations in the five desmosomal genes, genetic testing by means of Next Generation Sequencing was carried out on the proband. A heterozygous missense mutation in LDB3 c.1051A>G was identified. This result was confirmed by subsequent Sanger DNA sequencing. Another six carriers were identified amongst her relatives. Three subjects fulfilled the criteria for a definitive diagnosis of ARVC and one reached a borderline diagnosis. In conclusion, this is the first family with ARVC where a mutation in LDB3 is associated with ARVC. Next generation sequencing arises as a particular useful tool to point to new causative genes in ARVC.Entities:
Keywords: Cypher/ZASP; LDB3; arrhythmogenic right ventricular cardiomyopathy; next generation sequencing
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Year: 2014 PMID: 25041374 DOI: 10.1111/cge.12458
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438