Sudden onset of nephrotic syndrome in an asymptomatic Fabry patient: a case report

BACKGROUND: Fabry disease (FD) is an X-linked lysosomal storage disorder caused by the mutation of the GLA gene, encoding the α-galactosidase, which is responsible for the catabolism of neutral glycosphingolipids. Microalbuminuria or low-grade proteinuria, and continuously progressive renal failure...

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Detalles Bibliográficos
Autores principales: Zhang, Ruixiao, Chen, Zeqing, Lang, Yanhua, Shao, Shihong, Cai, Yan, You, Qingqing, Sun, Yan, Wang, Sai, Shi, Xiaomeng, Liu, Zhiying, Guo, Wencong, Han, Yue, Shao, Leping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534191/
https://www.ncbi.nlm.nih.gov/pubmed/32924720
http://dx.doi.org/10.1080/0886022X.2020.1818578

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534191/
https://www.ncbi.nlm.nih.gov/pubmed/32924720
http://dx.doi.org/10.1080/0886022X.2020.1818578

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