Syndrom VEXAS – objasnění komplexního autoinflamatorního onemocnění
Published in:
Transfuze Hematol. dnes,30, 2024, No. 2, p. 79-80.
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Editorial
Sources
1. Beck DB, Ferrada MA, Sikora KA, et al. Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease. N Engl J Med. 2020; 383 (27): 2628–2638.
2. Ciferska H, Gregová M, Klein M, et al. VEXAS syndrome: a report of three cases. Clin Exp Rheumatol. 2022; 40 (7): 1449.
3. Adam Z, Mayer J, Frič D, et al. VEXAS syndrom – nově popsané autoinflamatorní onemocnění s hematologickými symptomy. Popis případu a přehled literatury. Transfuze Hematol Dnes. 2024; 30 (2): prosím doplnit stránky.
4. Vostrý M, Stibůrková B, Mann H, et al. VEXAS syndrom – diagnóza na pomezí revmatologie a hematologie. Transfuze Hematol Dnes. 2024; 30 (2): prosím doplnit stránky.
5. Kobak S. VEXAS syndrome: Current clinical, diagnostic and treatment approaches. Intractable Rare Dis Res. 2023; 12 (3): 170–179.
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Haematology Internal medicine Clinical oncologyArticle was published in
Transfusion and Haematology Today
2024 Issue 2
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