Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy

Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy

<i>USH2A</i> 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 patie...

Full description

Bibliographic Details
Main Authors: Ana Fakin, Maja Šuštar, Jelka Brecelj, Crystel Bonnet, Christine Petit, Andrej Zupan, Damjan Glavač, Martina Jarc-Vidmar, Saba Battelino, Marko Hawlina
Format: Article
Language:English
Published: MDPI AG 2019-11-01
Series:Genes
Subjects:
ush2a
usher syndrome
retinitis pigmentosa
fundus autofluorescence
double hyperautofluorescent rings
electrophysiology
cone-rod dystrophy
Online Access:https://www.mdpi.com/2073-4425/10/12/956

Internet

https://www.mdpi.com/2073-4425/10/12/956

Similar Items