Genetic and clinical characteristics of skeletal and cardiac muscle in patients with lamin A/C gene mutations

Muscle Nerve. 2013 Aug;48(2):161-70. doi: 10.1002/mus.23827. Epub 2013 Jun 28.

Abstract

Alterations of the lamin A/C (LMNA) gene are associated with different clinical entities, including disorders that affect skeletal and cardiac muscle, peripheral nerves, metabolism, bones, and disorders that cause premature aging. In this article we review the clinical and genetic characteristics of cardiac and skeletal muscle diseases related to alterations in the LMNA gene. There is no single explanation of how LMNA gene alterations may cause these disorders; however, important goals have been achieved in understanding the pathogenic effects of LMNA gene mutations on cardiac and skeletal muscle.

Keywords: LMNA gene; cardiac muscle; peripheral nerve; premature aging; skeletal muscle.

Publication types

  • Review

MeSH terms

  • Animals
  • Humans
  • Lamin Type A / genetics*
  • Muscle, Skeletal / pathology*
  • Muscular Diseases / classification
  • Muscular Diseases / genetics*
  • Muscular Diseases / pathology*
  • Mutation / genetics*
  • Myocardium / pathology*

Substances

  • Lamin Type A