• 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. An autosomal recessive inheritance is proposed.
(Arch Ophthalmol 95:1190-1196, 1977)
Lewis RA, Lee GB, Martonyi CL, Barnett JM, Falls HF. Familial Foveal Retinoschisis. Arch Ophthalmol. 1977;95(7):1190–1196. doi:10.1001/archopht.1977.04450070088006
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