Early-onset autosomal dominant retinitis pigmentosa with severe hyperopia

B. L. Lam, G. F. Judisch

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

We studied a four-generation family with early-onset autosomal dominant retinitis pigmentosa, severe hyperopia, and axial eye lengths of less than 20 mm. The affected members had decreased vision, night blindness, typical peripheral retinal pigmentary changes, and electroretinographic abnormalities characteristic of retinitis pigmentosa. This pedigree suggests there is another variant of retinitis pigmentosa associated with hyperopia besides Leber's congenital amaurosis and preserved para-arteriole retinal pigment epithelium.

Original languageEnglish (US)
Pages (from-to)454-456
Number of pages3
JournalAmerican journal of ophthalmology
Volume111
Issue number4
DOIs
StatePublished - Jan 1 1991
Externally publishedYes

ASJC Scopus subject areas

  • Ophthalmology

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