In this study, we report three patients in the same family who have different clinical featuresand SD-OCT findings.
📌 3 Key Takeaways
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Objective & Hypothesis:X-linked juvenile retinoschisis (XLRS) is an X-linked hereditary retinal dystrophy characterized by splitting of the neurosensory retina.On fundus examination, the macula often has a spoke wheel appearance with foveal cystic lesions, and separation of the retinal layers istypical on spectral-domain optical coherence tomography (SD-OCT).
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Key Findings & Data:Patients with XLRS can exhibit different clinical courses, stages,and SD-OCT findings, even among members of the same family.
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Conclusion & Impact:In this study, we report three patients in the same family who have different clinical featuresand SD-OCT findings.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
X-linked juvenile retinoschisis (XLRS) is an X-linked hereditary retinal dystrophy characterized by splitting of the neurosensory retina.On fundus examination, the macula often has a spoke wheel appearance with foveal cystic lesions, and separation of the retinal layers istypical on spectral-domain optical coherence tomography (SD-OCT). Patients with XLRS can exhibit different clinical courses, stages,and SD-OCT findings, even among members of the same family. SD-OCT is an important imaging method that allows us to achievemore detailed information about XLRS. In this study, we report three patients in the same family who have different clinical featuresand SD-OCT findings.
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Cite This Article
ŞEKEROĞLU, M. A., YILMAZBAŞ, P., ANAYOL, M. A., DOĞUİZİ, S., ÇOLAK, S. (2022). Assessment of Spectral-Domain Optical Coherence Tomography Findings in Three Cases of X-Linked Juvenile Retinoschisis in the Same Family. Türk Oftalmoloji Dergisi, Cilt: 47 - Sayı: 5, 302–305. https://ajindex.com/articles/637854
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