Progressive cone dystrophy and sensorineural hearing loss

Bull Soc Belge Ophtalmol. 2004:(294):35-42.

Abstract

A 39-year old man presented 13 years ago with a history of progressive loss of vision and photophobia. A full ophthalmological and ENT work-up during several years of follow-up, including psychophysical as well as electrophysiological tests, revealed a progressive cone dystrophy in combination with sensorineural hearing loss. His younger sister presented with very similar features and underwent the same work-up. A novel syndrome of progressive cone dystrophy and sensorineural hearing loss is described in both siblings. Both also suffered from non-ocular disease possibly related to ciliary dysfunction. The condition is likely to be inherited as an autosomal recessive trait.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Female
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Male
  • Photophobia / genetics*
  • Retinal Cone Photoreceptor Cells
  • Retinal Degeneration / genetics*
  • Scotoma / genetics
  • Syndrome