Hypocomplementemic Atypical IgA Vasculitis: A Case Report

• Autors principals: Melvin Chan (Autor), Melisha Gayle Hanna (Autor), Nicholas Willard (Autor), Amy Treece (Autor), Bradley Patton Dixon (Autor)
• Format: Llibre
• Publicat: Frontiers Media S.A., 2022-06-01T00:00:00Z.
• Matèries: article
• Accés en línia: Connect to this object online.

IgA vasculitis (IgAV, also known as Henoch-Schönlein purpura or HSP) is a vasculitis of small vessels involving multiple organs, particularly of the joints, gastrointestinal tract, skin, and kidneys. Growing laboratory evidence has shown that complement plays a key role in the pathogenesis of IgAV,...