ReviewInternational journal of retina and vitreous2017
Multi-modal imaging and anatomic classification of the white dot syndromes.
Review in International journal of retina and vitreous, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
25 citing papers in PubMed.
- Non-Infectious Choroiditis Subdivided into Its Diverse Pathophysiological Sub-Groups Is the Best-Known and Most Appropriate Nomenclature to Date for the Reclassification and Diagnosis of Former White Dot Entities.Diagnostics (Basel, Switzerland) · 2026Review
- Acute macular neuroretinopathy: is the name still appropriate?Medical hypothesis, discovery & innovation ophthalmology journal · 2026Review
- Relentless Placoid Chorioretinitis: A Differential Diagnosis and Management Approach in a Challenging Case.Cureus · 2025Article
- Article
- Multiple evanescent white dot syndrome and presentations similar to multiple evanescent white dot syndrome in other disorders: a narrative review.International journal of ophthalmology · 2025Review
- Application of Ophthalmic Electrophysiology in Inflammatory Disorders of Retina and Optic Nerve.Journal of clinical medicine · 2024Review
- A case of secondary multiple evanescent white dot syndrome in a patient with preexisting wet age-related macular degeneration.American journal of ophthalmology case reports · 2024Article
- Unilateral acute posterior multifocal placoid pigment epitheliopathy (APMPPE) with delayed contralateral eye involvement.BMC ophthalmology · 2024Article
- Atypical case of acute posterior multifocal placoid pigment epitheliopathy with intraretinal fluid.BMJ case reports · 2023Article
- Unilateral Multiple Evanescent White Dot Syndrome-Like Reaction Following the CyberKnife Stereotactic Radiotherapy for Choroidal Malignant Melanoma.Turkish journal of ophthalmology · 2023Article
- Bilateral acute posterior multifocal placoid pigment epitheliopathy (APMPPE) following SARS-CoV-2 mRNA vaccine.BMJ case reports · 2022Article
- BTS clinical statement for the diagnosis and management of ocular tuberculosis.BMJ open respiratory research · 2022Review
- Case report: Visual snow as the presenting symptom in multiple evanescent white dot syndrome. Two case reports and literature review.Frontiers in neurology · 2022Article
- Acute posterior multifocal placoid pigment epitheliopathy (APMPPE).Journal of ophthalmic inflammation and infection · 2021Review
- Multimodal imaging supporting the pathophysiology of white dot syndromes.Journal of ophthalmic inflammation and infection · 2021Review
- [Choroidal neovascularization due to a punctate inner choroidopathy visualized by optical coherence tomography angiography].Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft · 2021Article
- Classification Criteria for Multifocal Choroiditis With Panuveitis.American journal of ophthalmology · 2021Article
- Visual acuity loss and development of ocular complications in white dot syndromes: a longitudinal analysis of 3 centers.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2019Article
- Repeatability of Optical Coherence Tomography Angiography in Uveitic Eyes.Translational vision science & technology · 2019Article
- Imageology features of different types of multifocal choroiditis.BMC ophthalmology · 2019Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The white dot syndromes (WDS) are a diverse group of posterior uveitidies that share similar clinical findings but are unique from one another. Multimodal imaging has allowed us to better understand the morphology, the activity and age of lesions, and whether there is CNV associated with these different ocular pathologies. The "white dot syndromes" and their uveitic masqueraders can now be anatomically categorized based on lesion localization. The categories include local uveitic syndromes with choroidal pathology, systemic uveitic syndromes with choroidal pathology, and multifocal choroiditis with outer retinal/choriocapillaris pathology with uveitis and without uveitis. Neoplastic and infectious etiologies are also discussed given their ability to masquerade as WDS.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.