[Differential diagnosis of juvenile normal pressure glaucoma]

Ophthalmologe. 2017 Sep;114(9):828-831. doi: 10.1007/s00347-016-0407-5.
[Article in German]

Abstract

The case of a 50-year-old female patient with autosomal dominant optic atrophy is described, which was initially misinterpreted and treated as normal pressure glaucoma. Bilateral partial optic atrophy can be diagnosed by chance with mild manifestation of symptoms and can initially be misinterpreted as glaucoma. Taking a detailed medical history and performing a thorough optic nerve head examination can raise the suspicion of hereditary optic atrophy. The reliable detection of autosomal dominant optic atrophy by genetic investigations should be strived for in such cases.

Keywords: Autosomal dominant; Glaucoma; Hereditary; Normal pressure glaucoma; Optic atrophy.

Publication types

  • Case Reports

MeSH terms

  • Chromosome Aberrations*
  • Diagnosis, Differential
  • Evoked Potentials, Visual / drug effects
  • Evoked Potentials, Visual / physiology
  • Female
  • Humans
  • Low Tension Glaucoma / diagnosis*
  • Low Tension Glaucoma / drug therapy
  • Low Tension Glaucoma / genetics
  • Low Tension Glaucoma / physiopathology
  • Magnetic Resonance Imaging
  • Medical History Taking
  • Middle Aged
  • Optic Atrophy, Autosomal Dominant / diagnosis*
  • Optic Atrophy, Autosomal Dominant / genetics
  • Optic Atrophy, Autosomal Dominant / physiopathology
  • Sulfonamides / therapeutic use
  • Thiazines / therapeutic use

Substances

  • Sulfonamides
  • Thiazines
  • brinzolamide