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March 1987

Congenital Stationary Night Blindness Presenting as Leber's Congenital Amaurosis

Author Affiliations

From the Departments of Ophthalmology (Drs Weleber and Tongue) and Medical Genetics (Dr Weleber), Oregon Health Sciences University, Portland.

Arch Ophthalmol. 1987;105(3):360-365. doi:10.1001/archopht.1987.01060030080031

• Two siblings with autosomal-recessive congenital stationary night blindness were clinically blind in infancy. Both had markedly abnormal electroretinograms that, in the first child, led consultants at two university centers to make the diagnosis of Leber's congenital amaurosis. The patients had intermittent nystagmus and esotropia, but good photopic vision developed eventually. Scotopic vision was clearly defective in each child. Refractive error in both patients was close to emetropic in early infancy but became myopic by 1 year of age. Congenital stationary night blindness must be considered in the differential diagnosis of the blind infant.

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