Primary photoreceptor degenerations: Retinitis pigmentosa

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Retinitis pigmentosa (RP) is caused by a large number of genetic defects that result in a characteristic pattern of degeneration of the rod and cone photoreceptors and the retinal pigment epithelium. RP is a heterogenous disease that can be classified in different ways. This article discusses the different categorizations of RP based on inheritance, genetic defect, and clinical presentation.

Original languageEnglish (US)
Title of host publicationEncyclopedia of the Eye
PublisherElsevier
Pages502-515
Number of pages14
ISBN (Electronic)9780123742032
ISBN (Print)9780123741981
DOIs
StatePublished - Jan 1 2010

Keywords

  • Bardet-Biedl syndrome
  • Bone spicules
  • Cone dystrophy
  • Cone-rod dystrophy
  • Dark adaptation
  • ERG
  • Electroretinogram
  • Leber congenital amaurosis
  • Pigmentary retinopathy
  • Retinal degeneration
  • Retinal dystrophy
  • Retinitis pigmentosa
  • Rod-cone dystrophy
  • Syndromic retinitis pigmentosa
  • Usher syndrome
  • Visual fields

ASJC Scopus subject areas

  • Medicine(all)

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