Renal manifestations in hypocomplementic urticarial vasculitis syndrome: Is it a distinct pathology?
Hypocomplementic urticarial vasculitis syndrome (HUVS) is an autoimmune disease characterized by recurrent urticaria, arthritis, and glomerulonephritis (GN).Anti-C1q antibody is the marker of HUVS together with low levels of classical pathway complements which are C2, C3, nitrile gloves in a bucket C4, and C1q.We report a case of a 6-year-old boy w