[Skip to Content]
[Skip to Content Landing]
Article
July 1977

Familial Foveal Retinoschisis

Arch Ophthalmol. 1977;95(7):1190-1196. doi:10.1001/archopht.1977.04450070088006
Abstract

• 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)

×