Autosomal Dominantly Inherited Macular Dystrophy with Preferential Short-Wavelength Sensitive Cone Involvement
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2012, Pediatric Ophthalmology and Strabismus: Expert Consult - Online and PrintProgressive Cone and Cone-Rod Dystrophies: Phenotypes and Underlying Molecular Genetic Basis
2006, Survey of OphthalmologyCitation Excerpt :Exceptions to this are cases where there is a predominant involvement of L-cones leading to a protan (red) color vision phenotype.83,167 Autosomal dominant cone dystrophy pedigrees with early tritan (blue) color vision defects have also been reported.18,205 Fundus examination may show a typical bull's-eye maculopathy (Fig. 2).
Alterations of L- and M-cone driven ERGs in cone and cone-rod dystrophies
2003, Vision ResearchThe assessment of L- and M-cone specific electroretinographical signals in the normal and abnormal human retina
2003, Progress in Retinal and Eye ResearchCone dystrophy, childhood vision impairment and education: are clinical measures of visual function adequate to support a child through education?
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This study was supported in part by National Eye Institute grants ROI-EY03084 (Dr. Bresnick), ROI-EY00901 (Dr. Pokorny), and ROI-EY01876 (Dr. Smith).
Reprint requests to George H. Bresnick, M.D., Department of Ophthalmology, 600 Highland Ave., Madison, WI 53792.
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