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Assessment of RS1 in X-Linked Juvenile Retinoschisis and Sporadic Senile Retinoschisis
Clinical Genetics, 1999 The RS1 gene is the causative gene in X-linked juvenile retinoschisis (RS). We have screened this gene for mutations in 13 patients with RS and in 7 probands with senile retinoschisis, a sporadic, later-onset form of retinoschisis.
Bernhard H Weber +2 more
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Ophthalmic Genetics, 2020 Background: Juvenile X-linked Retinoschisis (JXLRS) is a hereditary retinopathy that commonly presents with macular retinoschisis. In this study, we describe a group of patients who presented with peripheral retinoschisis with no macular schisis ...
Audina M Berrocal +2 more
exaly +2 more sources
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Acta Ophthalmologica, 1981
Four generations of a family with congenital retinoschisis are described. Six male members in the second generation suffer from this disease. The fundus changes in these patients were advanced with marked chorioretinal atrophy. Schisis of the retina was only seen in one of them.
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Four generations of a family with congenital retinoschisis are described. Six male members in the second generation suffer from this disease. The fundus changes in these patients were advanced with marked chorioretinal atrophy. Schisis of the retina was only seen in one of them.
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Archives of Ophthalmology, 1981
• Secondary retinoschisis is an unusual complication of chronic peripheral uveitis. Photocoagulation can be used to confirm the diagnosis.
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• Secondary retinoschisis is an unusual complication of chronic peripheral uveitis. Photocoagulation can be used to confirm the diagnosis.
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Nanophthalmos and Acquired Retinoschisis
American Journal of Ophthalmology, 2009To report three cases of nanophthalmos associated with acquired (senile) retinoschisis.Observational case series.Complete ophthalmologic evaluation (including funduscopy with scleral indentation, total axial length measurement with A-scan, optical coherence tomography [Stratus 3 OCT; Carl Zeiss Meditec Inc, Dublin, California, USA], and fundus ...
Elona, Dhrami-Gavazi +2 more
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Surgical management of retinoschisis
Current Opinion in Ophthalmology, 1997Most cases of X-linked juvenile retinoschisis and degenerative retinoschisis never require any type of surgical intervention. However, on rare occasions, associated problems such as retinal detachment come about and threaten the visual prognosis. Both conditions have in common the adherence of cortical vitreous to the inner layer of peripheral schisis ...
C D, Regillo, P H, Custis
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Ophthalmic Surgery, Lasers and Imaging Retina, 2007
<P>A 34-year-old woman with a refraction of -11 diopters in both eyes presented with a central scotoma and metamorphopsia in her right eye related to a juxtafoveal hemorrhage. Fluorescein angiography ruled out choroidal neovascularization and lacquer cracks.
M Rosa, Sanabria, Rosa M, Coco
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<P>A 34-year-old woman with a refraction of -11 diopters in both eyes presented with a central scotoma and metamorphopsia in her right eye related to a juxtafoveal hemorrhage. Fluorescein angiography ruled out choroidal neovascularization and lacquer cracks.
M Rosa, Sanabria, Rosa M, Coco
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Archives of Ophthalmology, 1977
Three young women, offspring of a nonconsanguineous marriage of normal parents, manifested mild visual loss associated with a bilateral foveal dystrophy that resembled the macular involvement in juvenile sex-linked retinoschisis. Electrophysiologic and psychophysiologic tests showed less severe involvement than the gonosomal equivalent.
R A, Lewis +4 more
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Three young women, offspring of a nonconsanguineous marriage of normal parents, manifested mild visual loss associated with a bilateral foveal dystrophy that resembled the macular involvement in juvenile sex-linked retinoschisis. Electrophysiologic and psychophysiologic tests showed less severe involvement than the gonosomal equivalent.
R A, Lewis +4 more
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COMPLICATED CONGENITAL RETINOSCHISIS
RETINAL Cases & Brief Reports, 2017Purpose: To describe the treatment and natural history of a patient with complicated congenital retinoschisis. Methods: A retrospective case report. A 10-month-old boy with congenital retinoschisis presented with tractional retinal detachments and foveal schisis in both eyes.
Brian T, Savoie, Philip J, Ferrone
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