The Phenotype of Early-Onset Retinal Degeneration in Persons withRDH12Mutations

Andreas Schuster, Andreas R. Janecke, Robert Wilke, Eduard Schmid, Debra A. Thompson, Gerd Utermann, Bernd Wissinger, Eberhart Zrenner, Andreas Gal
2007 Investigative Ophthalmology and Visual Science  
PURPOSE. To describe the retinal dystrophy phenotype associated with mutations in RDH12, the gene encoding a retinoid dehydrogenase/reductase expressed in the photoreceptor cells. METHODS. Sixteen persons from 12 families with pathogenic RDH12 mutations on both alleles were studied. Retinal phenotypes were characterized by ophthalmic examination, including psychophysical and standardized electrophysiological methods and multifocal electroretinography (mfERG). was diagnosed initially as Leber
more » ... genital amaurosis (LCA) or early-onset retinitis pigmentosa. These individuals appeared to share a common clinical picture, independent of the type of mutation, characterized by poor, yet useful visual function in early life, followed by progressive decline due to both rod and cone degeneration. Marked pigmentary retinopathy, including bone spicules in the peripheral retina, was present in all persons older than age 6, and pronounced maculopathy was evident in persons older than 7 years. A unique view into the progressive nature of the disorder was achieved by evaluation of seven affected persons from three consanguineous families, all carrying the homozygous p.Y226C mutation. CONCLUSIONS. Ophthalmic findings in persons with RDH12 mutations suggest that RDH12 loss-of-function results in a characteristic form of early and progressive rod-cone degeneration distinct from that caused by mutations in other LCA genes. From our data, it seems likely that various clinical designations appropriately describe the diagnosis in these persons, including early-onset retinitis pigmentosa, LCA type II, and childhood retinal dystrophy. (Invest Ophthalmol Vis Sci.
doi:10.1167/iovs.06-0628 pmid:17389517 fatcat:ssrv7vvz3jgllbowctwndrcnfe