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Publikováno v:
BMJ Case Rep
Hypocomplementemic urticarial vasculitis syndrome (HUVS) is a rare autoimmune disorder characterised by recurrent urticarial lesions and acquired hypocomplementemia with systemic manifestations. The authors present the case of a 70-year-old man who p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::172dc14dc9b92fa5294f3d7cc68621e8
https://doi.org/10.1136/bcr-2020-240041
https://doi.org/10.1136/bcr-2020-240041
