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Spectral-Domain Optical Coherence Tomography Analysis in Syndromic and Nonsyndromic Forms of Retinitis Pigmentosa due to USH2A Genetic Variants.

Ophthalmic research - 1 Jan 2022

Colombo Leonardo, Maltese Paolo Enrico, Romano Dario, Fogagnolo Paolo, Castori Marco, Marceddu Giuseppe, Cristofoli Francesca, Percio Marcella, Piteková Barbora, Modarelli Antonio Mattia, Bertelli Matteo, Rossetti Luca

Abstract excerpt

INTRODUCTION: This study aimed to analyze macular structure by using spectral-domain optical coherence tomography (SD-OCT) in a cohort of patients affected by autosomal recessive retinitis pigmentosa and Usher syndrome, due to genetic variants in USH2A gene, and to correlate optical coherence tomography (OCT) parameters with functional and genetic data. METHODS: The subjects of this study were 92 patients, 46...

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PMID: 34781295
DOI: 10.1159/000520329

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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