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

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 a...

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Bibliographic Details
Main Authors: Ruixiao Zhang, Zeqing Chen, Yanhua Lang, Shihong Shao, Yan Cai, Qingqing You, Yan Sun, Sai Wang, Xiaomeng Shi, Zhiying Liu, Wencong Guo, Yue Han, Leping Shao
Format: Article
Language:English
Published: Taylor & Francis Group 2020-01-01
Series:Renal Failure
Subjects:
fabry disease
gla gene
immunosuppressive treatment
nephrotic syndrome
variant
Online Access:http://dx.doi.org/10.1080/0886022X.2020.1818578

Internet

http://dx.doi.org/10.1080/0886022X.2020.1818578

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