[Hereditary optic atrophies]

Rev Neurol (Paris). 2010 Dec;166(12):959-65. doi: 10.1016/j.neurol.2010.07.033. Epub 2010 Nov 5.
[Article in French]

Abstract

Introduction: Hereditary optic neuropathies, resulting from retinal ganglion cell degeneration, are a heterogeneous group of diseases ranging from asymptomatic forms to legal blindness.

State of knowledge: Two most frequent phenotypes are Kjer's disease, an autosomal dominant optic atrophy caused by OPA1 gene mutations, and Leber's disease due to maternally inherited mitochondrial DNA mutations.

Prospects and conclusion: Both optic neuropathies usually isolated are sometimes associated with extraocular symptoms, especially neurological symptoms, thus justifying a systematic neurological evaluation and brain imaging.

Publication types

  • English Abstract
  • Review

MeSH terms

  • DNA, Mitochondrial / genetics
  • GTP Phosphohydrolases / genetics
  • Humans
  • Mutation
  • Optic Atrophies, Hereditary / diagnosis
  • Optic Atrophies, Hereditary / genetics*
  • Optic Atrophies, Hereditary / pathology*
  • Optic Atrophy, Autosomal Dominant / genetics
  • Optic Atrophy, Autosomal Dominant / pathology
  • Optic Atrophy, Hereditary, Leber / genetics
  • Optic Atrophy, Hereditary, Leber / pathology
  • Retinal Ganglion Cells / pathology

Substances

  • DNA, Mitochondrial
  • GTP Phosphohydrolases
  • OPA1 protein, human