Familial foveal retinoschisis
R. A. Lewis, G. B. Lee, C. L. Martonyi, J. M. Barnett and H. F. Falls
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.