Sneddon syndrome: under diagnosed disease, complex clinical manifestations and challenging diagnosis. A case-based review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy,Rheumatology
Link
https://link.springer.com/content/pdf/10.1007/s00296-020-04625-1.pdf
Reference30 articles.
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2. Fabiani G, Martins RF, Koppe GL, Demartini Z Jr, Gatto LAM (2018) Cognitive and psychiatric changes as first clinical presentation in Sneddon Syndrome. Dement Neuropsychol 12(2):216–219. https://doi.org/10.1590/1980-57642018dn12-020016
3. Bolayir E, Yilmaz A, Kugu N, Erdogan H, Akyol M, Akyuz A (2004) Sneddon's Syndrome: clinical and laboratory analysis of 10 cases. Acta Med Okayama 58(2):59–65. https://doi.org/10.18926/amo/32100
4. Tietjen GE, Al-Qasmi MM, Shukairy MS (2002) Livedo reticularis and migraine: a marker for stroke risk? Headache 42(5):352–355. https://doi.org/10.1046/j.1526-4610.2002.02106.x
5. Frances C, Papo T, Wechsler B, Laporte JL, Biousse V, Piette JC (1999) Sneddon syndrome with or without antiphospholipid antibodies. A comparative study in 46 patients. Medicine 78(4):209–219. https://doi.org/10.1097/00005792-199907000-00001
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3. Unusual case of retinal arterial branch occlusion: possible variant of Sneddon syndrome;Archivos de la Sociedad Española de Oftalmología (English Edition);2024-05
4. Un caso inusual de oclusión de rama arterial retiniana: posible variante del síndrome de Sneddon;Archivos de la Sociedad Española de Oftalmología;2024-05
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