The genetics of primary open-angle glaucoma: a review

Exp Eye Res. 2009 Apr;88(4):837-44. doi: 10.1016/j.exer.2008.11.003. Epub 2008 Nov 14.

Abstract

Glaucoma is the major cause of irreversible blindness worldwide. Primary open-angle glaucoma (POAG), as the most prevalent form of glaucoma, is a complex inherited disorder and affects more than 2 million individuals in the United States. It has become increasingly clear that a host of genetic as well as environmental factors are likely to contribute to the phenotype. A number of chromosomal and genetic associations have been reported for POAG. This review examines what is currently known about the underlying genetic structure, what remains to be learned, and how this may affect our medical management of this major blinding disease.

Publication types

  • Review

MeSH terms

  • Cell Cycle Proteins
  • Chromosome Mapping / methods
  • Cytoskeletal Proteins / genetics
  • Eye Proteins / genetics*
  • Genetic Linkage
  • Genetic Predisposition to Disease
  • Glaucoma, Open-Angle / genetics*
  • Glycoproteins / genetics
  • Humans
  • Membrane Transport Proteins
  • Mutation
  • Transcription Factor TFIIIA / genetics

Substances

  • Cell Cycle Proteins
  • Cytoskeletal Proteins
  • Eye Proteins
  • Glycoproteins
  • Membrane Transport Proteins
  • OPTN protein, human
  • Transcription Factor TFIIIA
  • WDR36 protein, human
  • trabecular meshwork-induced glucocorticoid response protein