Presumed Autoimmune Pigmented Paravenous Retinochoroidal Atrophy in a Female Patient Aged 69 Years-Reference-Cited by-同舟云学术

Presumed Autoimmune Pigmented Paravenous Retinochoroidal Atrophy in a Female Patient Aged 69 Years

Published:2023-08-17 Issue:8 Volume:141 Page:e231014
ISSN:2168-6165
Container-title:JAMA Ophthalmology
language:en
Short-container-title:JAMA Ophthalmol

Author:

Costa Celso¹,Marques João Pedro¹²³

Affiliation:

1. Ophthalmology Unit, Centro de Responsabilidade Integrada de Oftalmologia, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal

2. University Clinic of Ophthalmology, Faculty of Medicine, University of Coimbra, Coimbra, Portugal

3. Clinical Academic Center of Coimbra, Coimbra, Portugal

Abstract

This case report describes a diagnosis of presumed autoimmune pigmented paravenous retinochoroidal atrophy in a 69-year-old patient who presented with slowly progressive vision loss and nyctalopia.

Publisher

American Medical Association (AMA)

Subject

Ophthalmology

Link

https://jamanetwork.com/journals/jamaophthalmology/articlepdf/2808449/jamaophthalmology_costa_2023_ei_230017_1691537670.88928.pdf

Reference2 articles.

1. Pigmented paravenous retinochoroidal atrophy: a case report supported by multimodal imaging studies.;Jung;Medicina (Kaunas),2021

2. Pigmented paravenous retinochoroidal atrophy with acute angle-closure glaucoma and posterior subcapsular cataract: a case report.;Sun;BMC Ophthalmol,2022

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1. WITHDRAWN: Pigmented paravenous retinochoroidal atrophy caused by VPS13B gene mutations: a case report;2024-01-12

2. Pigmented paravenous retinochoroidal atrophy caused by VPS13B gene mutations: a case report;2023-12-02