ARVO Meeting Abstracts
 QUICK SEARCH:   [advanced]


This Article
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Vincent, A. L.
Right arrow Articles by Wong, F.
Right arrow Search for Related Content
Right arrow Articles by Vincent, A. L.
Right arrow Articles by Wong, F.
Invest Ophthalmol Vis Sci 2012;53: E-Abstract 4591.
© 2012 ARVO


Retinal Structure and Function in a Pedigree Cosegregating Achromatopsia and a Rhodopsin Mutation

Andrea L. Vincent1,2, Joseph Carroll3A, Gerald A. Fishman4, Dianne Sharp2, Phyllis Summerfelt3A, Vesper Williams3A, Alfredo Dubra3A, Adam M. Dubis3B and Fulton Wong5

1Ophthalmology, University of Auckland, Auckland, New Zealand
2Eye Department, Greenlane Clinical Centre, Auckland District Health Board, Auckland, New Zealand
AOphthalmology, BCellBiology, Neurobiology and Anatomy, 3Medical College of Wisconsin, Milwaukee, Wisconsin
4Pangere Center for the Study of Inherited Retinal Disease, Chicago Lthouse for the Blind & Vis Impaired, Chicago, Illinois
5Department of Ophthalmology, Duke University Eye Center, Durham, North Carolina

Commercial Relationships: Andrea L. Vincent, None; Joseph Carroll, Medical Advisory Board, Imagine Eyes, Inc (S); Gerald A. Fishman, None; Dianne Sharp, None; Phyllis Summerfelt, None; Vesper Williams, None; Alfredo Dubra, None; Adam M. Dubis, None; Fulton Wong, None

Support: FFB, RPB, NIH EY017607, Save Sight Society NZ, Retina NZ


Purpose:To characterize retinal structure and function in a family cosegregating CNGA3 and RHO F45L mutations, using electrophysiology and adaptive optics imaging. Recessive CNGA3 mutations manifest as achromatopsia (ACHM) that disrupts cone function, while a dominant rhodopsin mutation could potentially cause rod and cone dysfunction.

Methods:In one pedigree we identified two affected siblings with achromatopsia, with compound heterozygous mutations in CNGA3 detected on exome sequencing, which also detected a RHO F45L mutation. Cascade screening identified two adults with heterozygous CNGA3 L527R and RHO F45L mutations, one additional sibling with CNGA3 R227Cand RHO F45L and one adult with RHO F45L in isolation. RHO F45L is reported as a pathogenic cause of autosomal dominant retinitis pigmentosa in a number of families.(Berson et al. IOVS 2002;43:3027, Sung et al. PNAS 1991;88:6481). Comprehensive clinical examination included visual acuity, dilated fundus examination, electrophysiology (ERG), spectral domain optical coherence tomography (OCT), and adaptive optics scanning laser ophthalmoscopy (AO).

Results:Two affected children presented with nystagmus, photophobia, and poor vision (20/200-20/100). ERG showed normal scotopic function but nondetectable photopic function consistent with congenital ACHM. Retinal imaging was limited by nystagmus but AO images of the photoreceptor mosaic revealed reduced cone structure and an intact rod mosaic. Few wave-guiding cones were observed consistent with previous findings in ACHM. (Genead et al. IOVS 2011;52:7298) One child with CNGA3 R227Cand RHO F45L, and two adult carriers of CNGA3 L527R and RHO F45L had normal vision, fundus, ERG and OCT. AO images of the photoreceptor mosaic revealed complete cone and rod mosaics, with density of cones and rods within a normal range in all three. Examination of the isolated RHO F45L carrier was similarly normal but AO imaging was not undertaken.

Conclusions:Comprehensive clinical characterization in this pedigree suggests that RHO F45L is not pathogenic within this pedigree and in the context of a CNGA3 mutation background. The ability to characterize older family members with ERG, SD-OCT and AO provides considerable reassurance in this family that the young achromats would unlikely develop future rod dysfunction as a result of their RHO F45L mutation.

Keywords: genetics • retinal degenerations: hereditary • imaging/image analysis: clinical

© 2012, The Association for Research in Vision and Ophthalmology, Inc., all rights reserved. Permission to republish any abstract or part of an abstract in any form must be obtained in writing from the ARVO Office prior to publication.