Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1038/s41433-024-03432-3 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Coats-like vasculopathy in RDH12 Leber congenital amaurosis.
Eye (Lond)
October 2024
Department of Ophthalmology, Hospital Nord, Aix-Marseille University, Chemin des Bourrely, Marseille, France.
Eales' disease with secondary coats'-like reaction: a case report.
BMC Ophthalmol
September 2024
Department of Ophthalmology, Faculty of Medicine, 1UM Eye Research Centre (UMERC), Universiti Malaya, Kuala Lumpur, Malaysia.
Background: Eales' disease is an idiopathic, inflammatory condition characterized by peripheral retinal phlebitis, distal non-perfusion, and neovascularization. Coats' disease, on the other hand, is an idiopathic, retinal vasculopathy characterized by telangiectasia and yellowish exudation. Both diseases commonly affect males.
View Article and Find Full Text PDFCoats-Like Presentation of Familial Exudative Vitreoretinopathy Associated With a Novel Variant.
Ophthalmic Surg Lasers Imaging Retina
August 2024
This report describes a unique case of a Coats-like presentation of familial exudative vitreoretinopathy in an 11-year-old girl. The patient was originally referred for evaluation of presumed Coats disease and presented with telangiectatic vessels, perivascular exudates, diffuse peripheral exudation, and intraretinal hemorrhages. Clinical and angiographical findings were consistent with familial exudative vitreoretinopathy, while genetic testing identified variants of uncertain significance in two associated genes, and .
View Article and Find Full Text PDFCoats-like Vasculopathy in Inherited Retinal Disease: Prevalence, Characteristics, Genetics, and Management.
Ophthalmology
December 2023
Moorfields Eye Hospital, London, United Kingdom; UCL Institute of Ophthalmology, University College London, London, United Kingdom. Electronic address:
Article Synopsis
- This study focuses on a diverse group of 67 patients with inherited retinal disease (IRD)-related Coats-like vasculopathy (CLV), the largest cohort documented.
- The research involved reviewing clinical and genetic data to assess visual function and treatment responses, revealing that 54% of patients had isolated retinitis pigmentosa and most presented with significant retinal issues like exudative retinal detachment.
- Results showed a significant decline in visual acuity over time, with a considerable number of patients losing vision, highlighting the challenges in managing this condition.
Management of Coats-Like Disease in a Forty-Four-Year-Old Patient with FSHD Type I.
Case Rep Ophthalmol
June 2023
Clinica di Oftalmologia, Ospedale Regionale di Lugano, Ente Ospedaliero Cantonale (EOC), Lugano, Switzerland.
A forty-four-year-old female patient known for FSHD type I, with unremarkable past ocular history, complained of progressive visual acuity deterioration during a routine ophthalmological visit. Best-corrected visual acuity (BCVA) was 1.0 decimal Snellen equivalent bilaterally.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!