Assessment of Spectral-Domain Optical Coherence Tomography Findings in Three Cases of X-Linked Juvenile Retinoschisis in the Same Family
| Autor: | Mustafa Alpaslan Anayol, Pelin Yilmazbas, Sibel Doguizi, Mehmet Ali Sekeroglu, Salih Çolak |
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| Rok vydání: | 2016 |
| Předmět: |
medicine.medical_specialty
genetic structures lcsh:Medicine Spectral domain Case Report Fundus (eye) Hereditary retinal dystrophy chemistry.chemical_compound Optical coherence tomography lcsh:Ophthalmology Foveal Ophthalmology medicine Retina medicine.diagnostic_test business.industry lcsh:R X-linked juvenile retinoschisis Retinal eye diseases medicine.anatomical_structure chemistry lcsh:RE1-994 spectral-domain optical coherence tomography sense organs Juvenile retinoschisis business |
| Zdroj: | Turkish Journal of Ophthalmology Türk Oftalmoloji Dergisi, Vol 47, Iss 5, Pp 302-305 (2017) |
| ISSN: | 2149-8695 |
| Popis: | 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 is typical 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 achieve more detailed information about XLRS. In this study, we report three patients in the same family who have different clinical features and SD-OCT findings. |
| Databáze: | OpenAIRE |
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