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Bookmark or Share- X-Linked Retinoschisis - OphthalmologyWe assembled one of the largest XLRS cohorts to date with the aim of describing a detailed phenotypic spectrum, the long-term development of clinical characteristics, and potential genotype–phenotype correlations.
- X-linked juvenile retinoschisis: MedlinePlus GeneticsX-linked juvenile retinoschisis is a condition characterized by impaired vision that begins in childhood and occurs almost exclusively in males. Explore symptoms, inheritance, genetics of this condition.
- NEI Human Gene Therapy Trial for Retinoschisis UnderwayXLRS is a genetic disorder that causes splitting through the layers of the retina, the light-sensitive neural tissue in the back of the eye. XLRS gene mutations are inherited from mother to child; however, typically only males develop symptoms.
- X-Linked Retinoschisis (XLRS) - Foundation Fighting BlindnessX-linked retinoschisis (XLRS) is an inherited disease that causes loss of central and peripheral vision due to degeneration of the retina. The retina is a thin piece of tissue lining the back of the eye.
- X-linked Retinoschisis - EyeWikiX-linked Retinoschisis, or X-Linked Juvenile Retinoschisis is a rare congenital disease of the retina caused by mutations in the RS1 gene, which encodes retinoschisin, a protein involved in intercellular adhesion and likely retinal cellular organization.
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