Novel plakophilin2 mutation: three-generation family with arrhythmogenic right ventricular cardiomyopathy

Scand Cardiovasc J. 2012 Apr;46(2):72-5. doi: 10.3109/14017431.2011.636068. Epub 2011 Dec 8.

Abstract

Objectives: The autosomal dominant form of arrhythmogenic right ventricular cardiomyopathy (ARVC) has been linked to mutations in desmosomal proteins. A mutation in plakophilin 2 (PKP 2) is a frequent cause for ARVC. We describe a new mutation in the PKP2 gene, the genotype-phenotype variation in this mutation and its clinical consequences.

Design: Individuals in a three-generation family were investigated after the sudden cardiac death of a young male. Clinical evaluation, electrocardiography, echocardiography, magnetic resonance imaging, endomyocardial biopsy and genetic testing were performed.

Results: A novel heterozygote mutation, a c.368G > A transition, located in exon 3 of the PKP2 gene was found (p.Trp123X). The phenotype was characterized by arrhythmia at an early age in some individuals, with mild abnormalities on imaging.

Conclusions: This new plakophilin mutation demonstrates variable penetrance and phenotypic expression in ARVC, and highlights the need of genetic testing and thorough phenotype examination in ARVC pedigrees.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Arrhythmogenic Right Ventricular Dysplasia / genetics*
  • Child, Preschool
  • Death, Sudden, Cardiac
  • Fatal Outcome
  • Female
  • Genetic Predisposition to Disease
  • Genetic Testing
  • Humans
  • Male
  • Mutation
  • Pedigree
  • Phenotype
  • Plakophilins / genetics*

Substances

  • PKP2 protein, human
  • Plakophilins