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• W1968155207 abstract "purpose. To determine the underlying retinal micropathology in subclasses of autosomal dominant retinitis pigmentosa (ADRP) caused by rhodopsin (RHO) mutations. methods. Patients with RHO-ADRP (n = 17, ages 6–73 years), representing class A (R135W and P347L) and class B (P23H, T58R, and G106R) functional phenotypes, were studied with optical coherence tomography (OCT), and colocalized visual thresholds were determined by dark- and light-adapted chromatic perimetry. Autofluorescence imaging was performed with near-infrared light. Retinal histology in hT17M-rhodopsin mice was compared with the human results. results. Class A patients had only cone-mediated vision. The outer nuclear layer (ONL) thinned with eccentricity and was not detectable within 3 to 4 mm of the fovea. Scotomatous extracentral retina showed loss of ONL, thickening of the inner retina, and demelanization of RPE. Class B patients had superior–inferior asymmetry in function and structure. The superior retina could have normal rod and cone vision, normal lamination (including ONL) and autofluorescence of the RPE melanin; laminopathy was found in the scotomas. With Fourier-domain-OCT, there was apparent inner nuclear layer (INL) thickening in regions with ONL thinning. Retinal regions without ONL had a thick hyporeflective layer that was continuous with the INL from neighboring regions with normal lamination. Transgenic mice had many of the laminar abnormalities found in patients. conclusions. Retinal laminar abnormalities were present in both classes of RHO-ADRP and were related to the severity of colocalized vision loss. The results in human class B and the transgenic mice support the following disease sequence: ONL diminution with INL thickening; amalgamation of residual ONL with the thickened INL; and progressive retinal remodeling with eventual thinning." @default.
• W1968155207 created "2016-06-24" @default.
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• W1968155207 date "2008-04-01" @default.
• W1968155207 modified "2023-10-17" @default.
• W1968155207 title "Retinal Laminar Architecture in Human Retinitis Pigmentosa Caused by<i>Rhodopsin</i>Gene Mutations" @default.
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• W1968155207 doi "https://doi.org/10.1167/iovs.07-1110" @default.
• W1968155207 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3179264" @default.
• W1968155207 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18385078" @default.
• W1968155207 hasPublicationYear "2008" @default.
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