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  • Title: Familial foveal retinoschisis associated with a rod-cone dystrophy.
    Author: Noble KG, Carr RE, Siegel IM.
    Journal: Am J Ophthalmol; 1978 Apr; 85(4):551-7. PubMed ID: 306756.
    Abstract:
    A brother and sister born of a consanguinous marriage had bilateral foveal retinoschisis and a generalized rod-cone dysfunction. This was associated with nyctalopia, hyperopia, minimal vitreous opacities in the sister, a paramacular tapetal sheen reflex, normal retinal vessels, an abnormal electroretinogram, and a normal electro-oculogram in the less affected brother. Foveal retinoschisis is not pathognomonic for x-chromosome-linked juvenile retinoschisis. It may be seen as a manifestation of a macular dystrophy or associated with a generalized tapetoretinal dystrophy.
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