Retinitis pigmentosa is a common hereditary retinaldisease that leads to blindness.
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Lund said the same could be done in people with retinaldisease.
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However, few nonhuman primate models of genetic retinaldisease are known.
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Ultimately these tools should be useful in predicting retinaldisease progression.
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These successes notwithstanding, most other genetic retinaldisease will be refractory to supplementation.
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Congenital stationary night blindness (CSNB) is a nonprogressive retinaldisorder that can be associated with impaired night vision.
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Achromatopsia is an inherited retinaldisorder of cone photoreceptors characterized by markedly reduced visual acuity, extreme light sensitivity, and absence of color discrimination.
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Congenital stationary night blindness (CSNB) is a clinically and genetically heterogeneous group of non-progressive retinaldisorder with largely normal fundus appearance.
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Degeneration of RPE cells results in retinaldisorders such as age-related macular degeneration.
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Mutations in ABCA4 cause Stargardt disease and other blinding autosomal recessive retinaldisorders.
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Background: Many retinaldiseases are associated with vascular dysfunction accompanied by neuroinflammation.
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These results may help as we begin to understand certain age-related retinaldiseases.
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Furthermore, implications drawn from these models for gene therapy in retinaldiseases are discussed.
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Specific cone-directed therapy is of high priority in the treatment of human hereditary retinaldiseases.
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The findings also suggest that the therapeutical possibilities of PARP inhibition should include retinaldiseases like RP.
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The impairment is not due to developmental retinaldefect.
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Methods: This prospective cross-sectional study included 24 children previously treated with VGB and monitored in early childhood by electroretinogram for VGB-attributed retinaldefects.