AUTHOR=Lowndes Rebecca , Molz Barbara , Warriner Lucy , Herbik Anne , de Best Pieter B. , Raz Noa , Gouws Andre , Ahmadi Khazar , McLean Rebecca J. , Gottlob Irene , Kohl Susanne , Choritz Lars , Maguire John , Kanowski Martin , Käsmann-Kellner Barbara , Wieland Ilse , Banin Eyal , Levin Netta , Hoffmann Michael B. , Morland Antony B. , Baseler Heidi A. TITLE=Structural Differences Across Multiple Visual Cortical Regions in the Absence of Cone Function in Congenital Achromatopsia JOURNAL=Frontiers in Neuroscience VOLUME=15 YEAR=2021 URL=https://www.frontiersin.org/journals/neuroscience/articles/10.3389/fnins.2021.718958 DOI=10.3389/fnins.2021.718958 ISSN=1662-453X ABSTRACT=
Most individuals with congenital achromatopsia (ACHM) carry mutations that affect the retinal phototransduction pathway of cone photoreceptors, fundamental to both high acuity vision and colour perception. As the central fovea is occupied solely by cones, achromats have an absence of retinal input to the visual cortex and a small central area of blindness. Additionally, those with complete ACHM have no colour perception, and colour processing regions of the ventral cortex also lack typical chromatic signals from the cones. This study examined the cortical morphology (grey matter volume, cortical thickness, and cortical surface area) of multiple visual cortical regions in ACHM (