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Published in 2021 at "Pediatric Nephrology"
DOI: 10.1007/s00467-021-04987-z
Abstract: Considering the fact that the IgA vasculitis (IgAV), formerly known as Henoch-Schönlein purpura, is the most common systemic vasculitis in childhood, with an incidence fluctuating from 3 to 27 cases per 100 000 children [1,…
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Keywords:
nephrology;
genetics;
disease;
iga vasculitis ... See more keywords
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Published in 2018 at "Clinical Rheumatology"
DOI: 10.1007/s10067-018-4234-8
Abstract: Immunoglobulin A vasculitis (IgAV) is an immune complex, small vessel vasculitis with dominant IgA deposits in vessel walls, predominantly affecting the pediatric population. However, adults frequently have more severe gastrointestinal tract (GIT) and renal involvements…
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Keywords:
vasculitis;
igav patients;
inflammatory cell;
insight inflammatory ... See more keywords
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Published in 2023 at "Scandinavian Journal of Rheumatology"
DOI: 10.1080/03009742.2022.2154525
Abstract: Immunoglobulin A vasculitis (IgAV), formerly called Henoch–Schönlein purpura (HSP), predominantly affects small vessels, with deposition of immunoglobulin A complexes. The clinical manifestations include cutaneous purpura, arthralgia, gastrointestinal involvement, and glomerulonephritis (1). Childhood IgAV usually has…
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Keywords:
gastrointestinal involvement;
rtx;
treatment;
purpura abdominal ... See more keywords
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Published in 2019 at "Annals of the Rheumatic Diseases"
DOI: 10.1136/annrheumdis-2018-214142
Abstract: Background IgA vasculitis (IgAV, Henoch-Schönlein purpura) is a small-vessel vasculitis most common in children but also occurring in adults. Case series have suggested that IgAV may be associated with cardiovascular disease and venous thromboembolism, but…
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Keywords:
vasculitis;
adult onset;
disease;
cohort ... See more keywords