[X-chromosomal congenital retinoschisis. Clinical aspects and electrophysiology]

Fortschr Ophthalmol. 1990;87(3):264-8.
[Article in German]

Abstract

We evaluated retrospectively the clinical records and electrophysiological results of 52 patients suffering from X-linked congenital retinoschisis. Characteristic clinical findings were hyperopia (mean +2.3 +/- 3.1 D), reduced visual acuity (mean 0.24 +/- 0.2) and always macular pathology. Peripheral retinoschisis was present in 53% of the eyes. The natural course of the disease was normally stable. Complications were visual loss in 9.3%, vitreous hemorrhages in 4.7% and retinal detachments in 10.7% of the eyes. These complications generally occurred within the first decennium. Prophylactic laser coagulation was of no use because it was complicated by retinal detachment in 43% of our series. The electrooculogram was usually normal. In addition to the known electroretinographic findings of a low normal a-wave and reduced b-wave amplitudes, we found prolonged b-wave latencies and implicit times.

Publication types

  • English Abstract

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Electroretinography*
  • Female
  • Humans
  • Infant
  • Male
  • Retinal Degeneration / diagnosis
  • Retinal Degeneration / genetics*
  • Sex Chromosome Aberrations / genetics*
  • Visual Acuity / physiology
  • X Chromosome*