Advertisement
Logo
Search for

Volume 144, Issue 3, Pages 419-423.e2 (September 2007)


View previous. 15 of 51 View next.

Unusual Manifestations of X-Linked Retinoschisis: Clinical Profile and Diagnostic Evaluation

Dhananjay ShuklaaCorresponding Author Informationemail address, Anand Rajendrana, Daniel Gibbsb, Balasubbu Suganthalakshmia, Kang Zhangb, Periasamy Sundaresana

Accepted 11 May 2007. published online 18 June 2007.

Purpose

To describe the unusual clinical manifestations and diagnostic evaluation of X-linked retinoschisis (XLR).

Design

Prospective, observational case series.

Methods

Eight patients with subnormal vision seeking treatment at a tertiary eye care center were evaluated clinically by optical coherence tomography (OCT) and electroretinography (ERG) in this prospective, noncomparative case series. Mutational screening was performed for the retinoschisin gene (RS1) by direct deoxyribonucleic acid (DNA) sequencing. The primary outcome measures were the clinical fundus findings and genetic results.

Results

The mean patient age was 16.4 years (range, two to 33 years). Family history was positive in seven patients. Four demonstrated atypical fundus findings of XLR bilaterally. Atypical features included macular dragging and distortion (seven eyes, five patients), macular pigmentary changes or scarring (five eyes; three patients), and bilateral exudative detachments (one patient). One patient had macular dragging and pigmentary changes bilaterally. ERG aided diagnosis in five patients: selective B-wave suppression was observed in all. OCT demonstrated typical retinal schitic cavities universally, including the eyes with macular dragging and scarring. Genetic studies confirmed the clinical diagnosis in all patients; two revealed novel mutations.

Conclusions

We identified unusual presentations of XLR with the help of ERG, OCT, family screening, and genetic analysis; OCT seems to be a consistent diagnostic aid across the clinical spectrum of XLR.

a Aravind Eye Hospital & Postgraduate Institute of Ophthalmology, Madurai, Tamil Nadu, India

b Department of Ophthalmology and Visual Sciences, Program in Human Molecular Biology & Genetics, Eccles Institute of Human Genetics, University of Utah Health Sciences Center, Salt Lake City, Utah.

Corresponding Author InformationInquiries to Dhananjay Shukla, Aravind Eye Hospital & Postgraduate Institute of Ophthalmology, 1 Anna Nagar, Madurai 625 020, Tamil Nadu, India

PII: S0002-9394(07)00482-5

doi:10.1016/j.ajo.2007.05.016


View previous. 15 of 51 View next.

Advertisement