Myeloid bodies caused by COQ2 mutation: a case of concurrent COQ2 nephropathy and IgA nephropathy

Immunoglobulin A (IgA) nephropathy, in the presence of myeloid bodies, has been reported in Fabry disease (FD). In this case, we excluded the diagnosis of FD by demonstrating the absence of mutation in the α-galactosidase A（GLA）gene. Our patient also denied any history of use of cationic amphiphilic...

Descripción completa

Detalles Bibliográficos
Autores principales: Ni, Hai-Feng, Yang, Yan, Li, Chun-Qing, Zhou, Tong-Zhou, Liu, Bi-Cheng, Wang, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Exceptional Cases
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162858/
https://www.ncbi.nlm.nih.gov/pubmed/34084467
http://dx.doi.org/10.1093/ckj/sfab043

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162858/
https://www.ncbi.nlm.nih.gov/pubmed/34084467
http://dx.doi.org/10.1093/ckj/sfab043

Ejemplares similares