Immunoglobulin A vasculitis (IgAV; formerly Henoch Schonlein Purpura) is the most
common form of childhood vasculitis. It can occur in any age and peaks around 4–6 years …

Glomerular disease, be it primary or secondary, occurring in the setting of systemic
autoimmune diseases, infections, drugs, or malignancy, affects individuals of all ages. In …

IgA vasculitis with nephritis (IgAVN) shares many pathogenetic features with IgA
nephropathy (IgAN). The purpose of this review is to describe our current understanding of …

Introduction: This systematic literature review analyzed published evidence on IgA
nephropathy (IgAN), focusing on US epidemiology, health-related quality of life (HRQoL) …

Many authors suggested that IgA Vasculitis (IgAV) and IgA Nephropathy (IgAN) would be
two clinical manifestations of the same disease; in particular, that IgAV would be the …

The clinical features of the kidney involvement in immunoglobulin A (IgA) vasculitis (IgAVN)
differ in children and adults for both clinical presentation and progression. IgAVN in children …

Background The disease course of adult immunoglobulin A (IgA) vasculitis (IgAV; Henoch–
Schönlein purpura) has not been well defined. Methods In a retrospective survey, we …

IgA nephropathy (IgAN) is characterized by glomerular deposition of immune complexes
(ICs) consisting of IgA1 with O-glycans deficient in galactose (Gd-IgA1) and Gd-IgA1-specific …

Human IgA is comprised of two subclasses, IgA1 and IgA2. Monomeric IgA (mIgA),
polymeric IgA (pIgA), and secretory IgA (SIgA) are the main molecular forms of IgA. The …

Abstract IgA nephropathy (IgAN) and IgA vasculitis-associated nephritis (IgAVN) are among
the most frequent childhood glomerular diseases and are characterized by significant …