Novel clinical manifestation of congenital X-linked retinoschisis

Arch Ophthalmol. 2012 Feb;130(2):255-7. doi: 10.1001/archopthalmol.2011.1352.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Electroretinography
  • Eye Proteins / genetics
  • Humans
  • Male
  • Mutation, Missense
  • Retinoschisis / congenital
  • Retinoschisis / diagnosis*
  • Retinoschisis / genetics
  • Tomography, Optical Coherence
  • Vision Disorders / diagnosis*
  • Visual Acuity
  • Visual Fields*
  • Vitreous Hemorrhage / diagnosis*

Substances

  • Eye Proteins
  • RS1 protein, human