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      Swept-source and optical coherence tomography angiography in patients with X-linked retinoschisis

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          Abstract

          Purpose

          To explore the structural features of juvenile X-linked retinoschisis (XLRS) using swept-source-optical coherence tomography (SS-OCT) and optical coherence tomography angiography (OCT-A).

          Design

          Retrospective, observational cross-sectional study.

          Patients and methods

          Nine patients (18 eyes) diagnosed with juvenile XLRS were included. SS-OCT and OCT-A were used to evaluate the characteristics of the inner/outer retina and the choroid.

          Results

          SS-OCT showed that the inner nuclear layer (INL) was the most commonly affected area (16/18 eyes; 89%). No significant differences in central macular thickness (CMT) or subfield choroidal thickness (SFCT) were evidenced between eyes (CMT: 364  μm in the right eye vs 320  μm in the left eye; SFCT: 305 vs 307  μm; P=0.895). Best-corrected visual acuity (BCVA) did not correlate with CMT (rs= −0.19; P=0.445) or SFCT (rs=0.06; P=0.795). BCVA was significantly correlated with the following defects: outer plexiform layer (OPL; rs=0.50; P=0.036); external limiting membrane (ELM; rs=0.65; P=0.003); ellipsoid portion of inner segment (EPIS; rs=0.67; P=0.002); and the cone outer segment tips (COST; rs=0.69; P=0.001). Schisis at the INL revealed a spoke-like pattern in the foveal region and a reticular pattern in the parafoveal region on en-face imaging. In cases in which the schisis affected the OPL, multiple polygonal hyporeflective cavities were observed in the foveal region.

          Conclusions

          The hyporeflective spaces on SS-OCT were primarily located at the INL and OPL. BCVA did not correlate with CMT or SFCT; however, ELM, EPIS, and COST defects were significantly correlated with worse BCVA. There was a positive correlation between age and SFCT.

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          Most cited references30

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          Is Open Access

          X-linked juvenile retinoschisis: clinical diagnosis, genetic analysis, and molecular mechanisms.

          X-linked juvenile retinoschisis (XLRS, MIM 312700) is a common early onset macular degeneration in males characterized by mild to severe loss in visual acuity, splitting of retinal layers, and a reduction in the b-wave of the electroretinogram (ERG). The RS1 gene (MIM 300839) associated with the disease encodes retinoschisin, a 224 amino acid protein containing a discoidin domain as the major structural unit, an N-terminal cleavable signal sequence, and regions responsible for subunit oligomerization. Retinoschisin is secreted from retinal cells as a disulphide-linked homo-octameric complex which binds to the surface of photoreceptors and bipolar cells to help maintain the integrity of the retina. Over 190 disease-causing mutations in the RS1 gene are known with most mutations occurring as non-synonymous changes in the discoidin domain. Cell expression studies have shown that disease-associated missense mutations in the discoidin domain cause severe protein misfolding and retention in the endoplasmic reticulum, mutations in the signal sequence result in aberrant protein synthesis, and mutations in regions flanking the discoidin domain cause defective disulphide-linked subunit assembly, all of which produce a non-functional protein. Knockout mice deficient in retinoschisin have been generated and shown to display most of the characteristic features found in XLRS patients. Recombinant adeno-associated virus (rAAV) mediated delivery of the normal RS1 gene to the retina of young knockout mice result in long-term retinoschisin expression and rescue of retinal structure and function providing a 'proof of concept' that gene therapy may be an effective treatment for XLRS. Copyright © 2012 Elsevier Ltd. All rights reserved.
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            Choroidal thickness in myopic and nonmyopic children assessed with enhanced depth imaging optical coherence tomography.

            We examined choroidal thickness (ChT) and its topographic variation across the posterior pole in myopic and nonmyopic children. A total of 104 children aged 10 to 15 years (mean age, 13.1 ± 1.4 years) had ChT measured using enhanced depth imaging optical coherence tomography (OCT). Of these children 40 were myopic (mean spherical equivalent, -2.4 ± 1.5 diopters [D]) and 63 were nonmyopic (mean, +0.3 ± 0.3 D). Two series of 6 radial OCT line scans centered on the fovea were assessed for each child. Subfoveal ChT and ChT across a series of parafoveal zones over the central 6 mm of the posterior pole were determined through manual image segmentation. Subfoveal ChT was significantly thinner in myopes (mean, 303 ± 79 μm) compared to nonmyopes (mean, 359 ± 77 μm, P 3 mm diameter, P < 0.001). Myopic children have significantly thinner choroids compared to nonmyopic children of similar age, particularly in central foveal regions. The magnitude of difference in choroidal thickness associated with myopia appears greater than would be predicted by a simple passive choroidal thinning with axial elongation.
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              Choroidal thickness in childhood.

              We examined choroidal thickness (ChT) and its spatial distribution across the posterior pole in pediatric subjects with normal ocular health and minimal refractive error.
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                Author and article information

                Journal
                Eye (Lond)
                Eye (Lond)
                Eye
                Nature Publishing Group
                0950-222X
                1476-5454
                April 2018
                05 January 2018
                : 32
                : 4
                : 707-715
                Affiliations
                [1 ] Department of Ophthalmology, Bellvitge University Hospital , Barcelona, Spain
                [2 ] Department of Ophthalmology, Sant Joan de Deu Hospital , Barcelona, Spain
                [3 ] Department of Ophthalmology, Sant Pau Hospital , Barcelona, Spain
                Author notes
                [* ] Department of Ophthalmology, Bellvitge University Hospital , Feixa Llarga, s/n, L'Hospitalet de Llobregat, Barcelona 08907, Spain Tel: +34 93 260 76 00; Fax: 34 93 260 75 33. E-mail: noelpdrn@ 123456gmail.com
                Article
                PMC5898861 PMC5898861 5898861 eye2017281
                10.1038/eye.2017.281
                5898861
                29303151
                3b85b311-d31e-416b-b274-5d28858b915b
                Copyright © 2018 Macmillan Publishers Limited, part of Springer Nature.
                History
                : 29 April 2017
                : 02 October 2017
                Categories
                Clinical Study

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