Congenital Stationary Night Blindness Presenting as Leber's Congenital Amaurosis

Richard G. Weleber

Research output: Contribution to journalArticlepeer-review

31 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)360-365
Number of pages6
JournalArchives of ophthalmology
Volume105
Issue number3
DOIs
StatePublished - Mar 1987

ASJC Scopus subject areas

  • Ophthalmology

Fingerprint

Dive into the research topics of 'Congenital Stationary Night Blindness Presenting as Leber's Congenital Amaurosis'. Together they form a unique fingerprint.

Cite this