Optical cross-sectional imaging of the macula with the retinal thickness analyzer in X-linked retinoschisis.
OBJECTIVE: To assess the morphologic characteristics of the foveal abnormality in juvenile X-linked retinoschisis using the scanning retinal thickness analyzer (RTA). This characteristic foveal abnormality is present in 83% to 100% of patients with X-linked retinoschisis and has not been demonstrated histopathologically. METHODS: The RTA is a noncontact imaging device. The RTA scans an obliquely oriented slit laser beam across the macula to obtain a series of optical cross sections, which are digitized. PARTICIPANTS: The RTA was used to examine 7 eyes of 5 patients with X-linked retinoschisis. RESULTS: The RTA demonstrated foveal schisis in all eyes examined. In 2 eyes of 2 patients, a single schisis cavity, with an inner leaf in a dome-shaped configuration, was present. In 4 eyes of 3 patients, a single schisis cavity containing fine strands was present. Some of these strands partially, and others completely, bridged the cavity. In 1 eye of 1 patient, 2 separate schisis cavities with bridging strands were present in the fovea. CONCLUSIONS: Scanning RTA is a noninvasive imaging modality capable of producing optical cross sections that demonstrate the extent and structural details of the foveal schisis in X-linked retinoschisis. Scanning RTA seems to be effective in the detection, characterization, and quantification of foveal schisis.
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- X Chromosome
- Retinal Degeneration
- Retina
- Ophthalmology & Optometry
- Macula Lutea
- Image Processing, Computer-Assisted
- Humans
- Genetic Linkage
- Fovea Centralis
- Eye Diseases, Hereditary
Citation
Published In
DOI
ISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- X Chromosome
- Retinal Degeneration
- Retina
- Ophthalmology & Optometry
- Macula Lutea
- Image Processing, Computer-Assisted
- Humans
- Genetic Linkage
- Fovea Centralis
- Eye Diseases, Hereditary