|
|||||
|
|
Peripapillary sparing in RDH12-associated Leber congenital amaurosis |
|
| Authors: | Aakriti Garg Winston Lee Jesse D. Sengillo Rando Allikmets Kartik Garg |
| Affiliation: | 1. Department of Ophthalmology, College of Physicians and Surgeons, Columbia University, New York, New York, USA;2. Department of Pathology and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, New York, USA;3. Jonas Children’s Vision Care and Bernard &4. Shirlee Brown Glaucoma Laboratory, Columbia University Medical Center, New York, New York, USA;5. State University of New York Downstate Medical Center, Brooklyn, New York, USA;6. Jonas Children’s Vision Care and Bernard & |
| Abstract: | Background: Peripapillary sparing is a characteristic that is traditionally described as pathognomonic for Stargardt disease. Materials and methods: We present a multimodal assessment of four Leber congenital amaurosis (LCA) cases with congenital macular atrophy and severely attenuated electroretinogram findings caused by bilallelic mutations in RDH12. Results: Fundus autofluorescence imaging revealed a general loss of retinal pigment epithelium across the macula except for the peripapillary region in both eyes of all patients. Spectral domain-optical coherence tomography confirmed relative preservation in this area along with retinal thinning and excavation throughout the rest of the macula. LCA was diagnosed based on clinical exam and retinal imaging, and subsequently confirmed with genetic testing. Conclusions: Peripapillary sparing is a novel phenotypic feature of RDH12-associated LCA. |
| Keywords: | Autofluorescence Leber congenital amaurosis peripapillary sparing RDH12 spectral domain optical coherence tomography |