Hypocomplementemic Atypical IgA Vasculitis: A Case Report

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,...

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Detalles Bibliográficos
Autores principales: Chan, Melvin, Hanna, Melisha Gayle, Willard, Nicholas, Treece, Amy, Dixon, Bradley Patton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218267/
https://www.ncbi.nlm.nih.gov/pubmed/35757129
http://dx.doi.org/10.3389/fped.2022.886371

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218267/
https://www.ncbi.nlm.nih.gov/pubmed/35757129
http://dx.doi.org/10.3389/fped.2022.886371

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