Syndromic retinitis pigmentosa: ERG and phenotypic changes

Klin Monbl Augenheilkd. 2005 Mar;222(3):186-90. doi: 10.1055/s-2005-857973.

Abstract

Purpose: Our aim was to review the phenotype and extent of ERG changes in syndromic RP (SRP).

Patients and methods: A retrospective review of charts of 82 patients seen over the last 20 years with SRP was carried out. Clinical data were compared with changes in ERG. Full-field ERGs comprised selective rod-driven, maximal dark-adapted mixed responses, and isolated cone-driven signals. Occasionally, ERGs were recorded under brief general anaesthesia. ERG changes were classified as normal, reduced or extinguished.

Results: Syndromic RP was diagnosed for the following entities: Usher (45 patients), Laurence-Moon-Bardet-Biedl (LMBB, 17 patients), Kearns-Sayre (10), Batten (6), Refsum (3), Senior-Loken (1). ERG changes varied in every subgroup and were therefore not specific for the syndromes.

Conclusion: There was wide variation of clinical presentation in SRP, much as seen in isolated RP, often without obvious ophthalmoscopic changes. ERG testing is a prerequisite for differential diagnosis as well as for early detection of multiple handicaps.

MeSH terms

  • Electroretinography*
  • Humans
  • Ophthalmoscopy
  • Phenotype*
  • Retinal Degeneration / diagnosis
  • Retinal Degeneration / genetics
  • Retinitis Pigmentosa / classification
  • Retinitis Pigmentosa / diagnosis*
  • Retinitis Pigmentosa / genetics*
  • Retrospective Studies
  • Syndrome