Article Text

Download PDFPDF
Unilateral retinitis pigmentosa: 30 years follow-up
  1. Julia M Weller,
  2. Georg Michelson,
  3. Anselm G Juenemann
  1. Department of Ophthalmology, University of Erlangen-Nuremberg, Erlangen, Germany
  1. Correspondence to Dr Julia M Weller, julia.weller{at}


This case report depicts the clinical course of a female patient with unilateral retinitis pigmentosa (RP), who presented first in 1984 at the age of 43 years. At the beginning, there were cells in the vitreous leading to the diagnosis of uveitis with vasculitis. Within 30 years, the complete clinical manifestation of RP developed with bone spicule-shaped pigment deposits, pale optic disc, narrowed arterioles, cystoid macular oedema, posterior subcapsular cataract, concentric narrowing of the visual field and undetectable electroretinogram signal. At the age of 72 years, there are still no signs of retinal dystrophy in the other eye.

View Full Text

Statistics from

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.