Concurrent retinitis pigmentosa and pigmented paravenous retinochoroidal atrophy phenotypes in the same patient

Concurrent retinitis pigmentosa and pigmented paravenous retinochoroidal atrophy phenotypes in the same patient

We report a unique case of a patient with retinitis pigmentosa (RP) phenotype in one eye and pigmented paravenous retinochoroidal atrophy (PPRCA) phenotype in the other eye. We describe in detail the symptoms, clinical findings, and investigations done for a 32-year-old Indian woman. This patient ha...

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Bibliographic Details
Main Authors: Dhanashree Ratra, Dhileesh P Chandrasekharan, P Aruldas, Vineet Ratra
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:Indian Journal of Ophthalmology
Subjects:
CRB1 gene mutation
hereditary disorders
night blindness
pigmented paravenous retinochoroidal atrophy
retinal degeneration
retinitis pigmentosa
unilateral retinal degeneration
Online Access:http://www.ijo.in/article.asp?issn=0301-4738;year=2016;volume=64;issue=10;spage=775;epage=777;aulast=Ratra

Internet

http://www.ijo.in/article.asp?issn=0301-4738;year=2016;volume=64;issue=10;spage=775;epage=777;aulast=Ratra

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