Phenotypic Patterns of Cardiomyopathy Caused by Mutations in the Desmin Gene. A Clinical and Genetic Study in Two Inherited Heart Disease Units

Rev Esp Cardiol (Engl Ed). 2015 Nov;68(11):1027-9. doi: 10.1016/j.rec.2015.07.007. Epub 2015 Oct 1.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Atrial Fibrillation
  • Atrioventricular Block / genetics
  • Atrioventricular Block / physiopathology
  • Cardiac Resynchronization Therapy
  • Cardiomyopathies / diagnostic imaging
  • Cardiomyopathies / genetics*
  • Cardiomyopathies / therapy
  • Cardiomyopathy, Dilated / diagnostic imaging
  • Cardiomyopathy, Dilated / genetics*
  • Cardiomyopathy, Dilated / therapy
  • Cardiomyopathy, Restrictive / diagnostic imaging
  • Cardiomyopathy, Restrictive / genetics*
  • Cardiomyopathy, Restrictive / therapy
  • Defibrillators, Implantable
  • Desmin / genetics*
  • Echocardiography
  • Family
  • Female
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Male
  • Middle Aged
  • Muscular Dystrophies / diagnostic imaging
  • Muscular Dystrophies / genetics*
  • Muscular Dystrophies / therapy
  • Pacemaker, Artificial
  • Phenotype
  • Sequence Analysis, DNA
  • Tachycardia, Ventricular
  • Young Adult

Substances

  • Desmin

Supplementary concepts

  • Myopathy, Myofibrillar, Desmin-Related