ReviewRheumatology international2021
Sneddon syndrome: under diagnosed disease, complex clinical manifestations and challenging diagnosis. A case-based review.
Review in Rheumatology international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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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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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
6 citing papers in PubMed, 12 citations in OpenAlex.
- Long-term clinical progression of Sneddon syndrome associated with antiphospholipid syndrome.Dementia & neuropsychologia · 2026Article
- Comprehensive insights of Sneddon syndrome: A clinical perspective.Journal of central nervous system disease · 2024Review
- Sneddon's syndrome concurrent with cerebral venous sinus thrombosis: A case report.World journal of clinical cases · 2023Article
- Sneddon syndrome: a rare cause of stroke hidden in plain sight.Acta neurologica Belgica · 2023Article
- The Relevance of Skin Biopsies in General Internal Medicine: Facts and Myths.Dermatology and therapy · 2022Review
- Inadequate response to antiplatelet therapy in Sneddon's syndrome. Time to re-evaluate management recommendations?Anais brasileiros de dermatologiaArticle
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Herein, we report a case-based review of the Sneddon Syndrome (SS), a rare chronic condition which affects small to medium blood vessels. It is known by its skin presentation, livedo racemosa (LRC), and the relapsing cerebrovascular events. However, neither LRC nor cerebrovascular events are exclusive to SS. A 36-year-old female with history of mitral valve prolapse, hypothyroidism, Raynaud phenomenon, hypertension, migraines, and four episodes of transient ischemic attacks (TIA), presented to our clinic with new skin findings, suggestive of LRC. Based on her previous history, current presentation and skin biopsy results, she was diagnosed with SS secondary to antiphospholipid syndrome. The present report illustrates the difficulty in recognizing SS and how the heterogeneity of the disease may be contributing to the difficulty making a distinct diagnosis.
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Registered trials
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