Cell biology of disease: Telomeropathies: an emerging spectrum disorder

J Cell Biol. 2014 May 12;205(3):289-99. doi: 10.1083/jcb.201401012.

Abstract

A constellation of related genetic diseases are caused by defects in the telomere maintenance machinery. These disorders, often referred to as telomeropathies, share symptoms and molecular mechanisms, and mounting evidence indicates they are points along a spectrum of disease. Several new causes of these disorders have been recently discovered, and a number of related syndromes may be unrecognized telomeropathies. Progress in the clinical understanding of telomeropathies has in turn driven progress in the basic science of telomere biology. In addition, the pattern of genetic anticipation in some telomeropathies generates thought-provoking questions about the way telomere length impacts the course of these diseases.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Animals
  • Genetic Diseases, Inborn / genetics*
  • Genetic Diseases, Inborn / metabolism
  • Genetic Predisposition to Disease
  • Humans
  • Neoplasms / genetics
  • Neoplasms / metabolism
  • Phenotype
  • Risk Factors
  • Syndrome
  • Telomere / metabolism*
  • Telomere Homeostasis*
  • Telomere Shortening*