Rare Collagenous Heterozygote Variants in Children With IgA Nephropathy

INTRODUCTION: Childhood IgA nephropathy (cIgAN) is a primary glomerulonephritis clinically characterized by microscopic hematuria and proteinuria, the presence of which may potentially overlap with Alport syndrome. Interestingly, earlier studies suggested that familial IgAN could be linked to the ch...

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Detalles Bibliográficos
Autores principales: Cambier, Alexandra, Robert, Thomas, Hogan, Julien, Rabant, Marion, Peuchmaur, Michel, Boyer, Olivia, Ulinski, Tim, Monteiro, Renato C., Mesnard, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116726/
https://www.ncbi.nlm.nih.gov/pubmed/34013111
http://dx.doi.org/10.1016/j.ekir.2021.02.022

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116726/
https://www.ncbi.nlm.nih.gov/pubmed/34013111
http://dx.doi.org/10.1016/j.ekir.2021.02.022

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