[Clinical practice guidelines for single gene glaucoma disorder]

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Mar 10;37(3):329-333. doi: 10.3760/cma.j.issn.1003-9406.2020.03.018.
[Article in Chinese]

Abstract

Glaucoma is a group of progressive optic neuropathies featuring retinal ganglion cell and axonal degeneration, which typically manifest as sunken atrophy of optic papilla and characteristic visual field defect. Genetic factors play an important role in the pathogenesis of glaucoma. This guideline mainly focuses on single gene mutation-related glaucoma by summarizing the pathogenic genes, disease diagnosis and clinical consultation of primary congenital glaucoma (PCG) and primary open-angle glaucoma (POAG), with an aim to regulate their molecular diagnosis, genetic counseling and treatment.

MeSH terms

  • Atrophy
  • Glaucoma / diagnosis*
  • Glaucoma / genetics*
  • Glaucoma / therapy*
  • Glaucoma, Open-Angle
  • Humans
  • Mutation
  • Optic Disk
  • Optic Nerve Diseases
  • Practice Guidelines as Topic*