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Article

Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy.

Genes - 21 Nov 2019

Fakin Ana, Šuštar Maja, Brecelj Jelka, Bonnet Crystel, Petit Christine, Zupan Andrej, Glavač Damjan, Jarc-Vidmar Martina, Battelino Saba, Hawlina Marko

Abstract excerpt

USH2A mutation is the most common cause of retinitis pigmentosa, with or without hearing impairment. Patients most commonly exhibit hyperautofluorescent ring on fundus autofluorescence imaging (FAF) and rod-cone dystrophy on electrophysiology. A detailed study of three USH2A patients with a rare pattern of double hyperautofluorescent rings was performed. Twenty-four patients with typical single...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 31766479
DOI: 10.3390/genes10120956
PMCID: PMC6947471

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Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy.PMID 31766479Read ↗

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