Journal of Health Sciences (Sep 2012)

Leber’s hereditary optic neuropathy - case report

  • Mirjana A. Janicijevic Petrovic,
  • Tatjana Sarenac Vulovic,
  • Nenad Petrovic,
  • Suncica Sreckovic,
  • Svetlana Paunovic,
  • Katarina Janicijevic,
  • Dejan Vulovic,
  • Dragan Vujic

Journal volume & issue
Vol. 2, no. 2
pp. 148 – 152

Abstract

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Leber’s hereditary optic neuropathy is a neuro-ophthalmological entity characterized by acute or subacute bilateral, not simultaneous visual loss with centro cekal scotoma and occasional further visual improvement. This rare ophthalmological disease can be accompanied with dyschromatopsia. It is associated with a matrilineal inheritance pattern. Its diagnosis used to be solely clini¬cal, aided by imaging and neuro-physiological studies, until the advent of descriptions of mitochondrial biochemical abnormalities and genetic testing. We describe a case of 24 year old male with progressive painless deterioration of visual acuity and positive family history.

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