Macular spectral-domain optical coherence tomography in patients with X linked retinoschisis

被引:50
作者
Gregori, N. Z. [1 ,2 ]
Berrocal, A. M. [1 ]
Gregori, G. [1 ]
Murray, T. G. [1 ]
Knighton, R. W. [1 ]
Flynn, H. W., Jr. [1 ]
Dubovy, S. [1 ]
Puliafito, C. A. [3 ]
Rosenfeld, P. J. [1 ]
机构
[1] Univ Miami, Miller Sch Med, Bascom Palmer Eye Inst, Dept Ophthalmol, Miami, FL 33136 USA
[2] Vet Affairs Med Ctr, Miami, FL 33125 USA
[3] Univ So Calif, Keck Sch Med, Dept Ophthalmol, Los Angeles, CA 90033 USA
基金
美国国家卫生研究院;
关键词
JUVENILE RETINOSCHISIS; GENE;
D O I
10.1136/bjo.2007.136127
中图分类号
R77 [眼科学];
学科分类号
100212 [眼科学];
摘要
Aim: To evaluate macular anatomy in patients with X linked retinoschisis (XLRS) using spectral-domain optical coherence tomography (SD-OCT). Methods: Consecutive observational case series. Clinical features were obtained through retrospective chart review. Only eyes without prior surgical interventions and those scanned with SD-OCT were included. The OCT images were analysed. Results: Fourteen eyes of seven males with XLRS scanned with SD-OCT, age 5 to 45 years, were identified. On clinical examination, stellate spoke-like cystic maculopathy was present in nine eyes, and an atrophic foveal lesion in five eyes. SD-OCT revealed cystoid spaces accounting for retinal splitting in the inner nuclear layer in 12 eyes, and outer plexiform layer in two eyes of one patient. A few small cysts, not accounting for the foveal splitting, were seen in the outer nuclear layer in four eyes and in the ganglion cell layer and/or nerve fibre layer in six eyes. Conclusions: SD-OCT localised the foveomacular retinoschisis in XLRS to the retinal layers deeper than the nerve fibre layer. In the present study, the foveomacular schisis was seen most frequently in the inner nuclear layer.
引用
收藏
页码:373 / 378
页数:6
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