Sneddon syndrome: under diagnosed disease, complex clinical manifestations and challenging diagnosis. A case-based review
Sign Up to like & getrecommendations! Published in 2020 at "Rheumatology International"
DOI: 10.1007/s00296-020-04625-1
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… read more here.
Keywords: case based; based review; sneddon syndrome; disease ... See more keywords
Sneddon syndrome: a comprehensive clinical review of 53 patients
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DOI: 10.1007/s00415-021-10407-x
Abstract: The presence of livedo reticularis in patients with ischaemic stroke is associated with Sneddon syndrome (SS). Our objective was to present the clinical features of SS patients and to assess the role of antiphospholipid antibodies… read more here.
Keywords: comprehensive clinical; clinical features; diagnosis; syndrome comprehensive ... See more keywords
Coexistence of scleromyxedema and Sneddon syndrome
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DOI: 10.1016/j.jdcr.2021.03.023
Abstract: MTHFR: methylenetetrahydrofolate reductase INTRODUCTION Scleromyxedema is a rare mucinosis characterized by a generalized, papular, sclerodermoid cutaneous eruption often accompanied by extracutaneous manifestation and associated with paraproteinemia. Sneddon syndrome is a progressive disease characterized by generalized… read more here.
Keywords: coexistence scleromyxedema; sneddon syndrome; scleromyxedema sneddon;
Echocardiographic features in antiphospholipid-negative Sneddon's syndrome and potential association with severity of neurological symptoms or recurrence of strokes: a longitudinal cohort study.
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DOI: 10.1093/ehjci/jez312
Abstract: AIMS Sneddon's syndrome (SS) may be classified as antiphospholipid positive (aPL+) or negative (aPL- SS). An association between Libman-Sacks (LS) endocarditis and strokes has been described in aPL+ patients. To describe cardiac involvement in aPL-… read more here.
Keywords: neurological symptoms; endocarditis; association; potential association ... See more keywords
Mitsuda psychosis and holodysphrenia revisited: An atypical psychosis in a patient with parieto‐occipital paroxysmal electroencephalographic activity and high unconjugated bilirubin
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DOI: 10.1111/pcn.12487
Abstract: psychiatric disorder. After admission, an initial treatment of oral haloperidol (1 mg/day) was administered, rather than second-generation antipsychotics (which are associated with tendency of metabolic syndrome and increased risk of stroke), along with a physical… read more here.
Keywords: sneddon syndrome; day; psychotic symptoms; psychosis ... See more keywords
Abstract WP476: Remarkable Hemorrhagic Imaging Manifestations Might Be Responsible for the Prominent Atrophy and Cognitive Decline in Sneddon Syndrome
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DOI: 10.1161/str.51.suppl_1.wp476
Abstract: Objective: Sneddon syndrome is a rare non-inflammatory arteriopathy affecting small and medium-sized arteries, characterized by a generalized livedo reticularis and recurrent ischemic stroke. Hemorrhagic stroke was reported in limited cases, but microbleeds and superficial siderosis… read more here.
Keywords: atrophy; superficial siderosis; sneddon syndrome; hemorrhagic imaging ... See more keywords
Freiberg’s Infarction as the First Clinical Presentation of Sneddon Syndrome
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DOI: 10.4103/jpn.jpn_159_19
Abstract: ABSTRACT Sneddon syndrome is a rare, non-inflammatory vasculopathy that generally occurs in the third to fourth decade of life but may rarely present in the pediatric population. It is characterized by the skin finding of… read more here.
Keywords: infarction first; first clinical; freiberg infarction; clinical presentation ... See more keywords