INF2 p.Arg214Cys mutation in a Chinese family with rapidly progressive renal failure and follow-up of renal transplantation: case report and literature review

INF2 p.Arg214Cys mutation in a Chinese family with rapidly progressive renal failure and follow-up of renal transplantation: case report and literature review

Abstract Background Heterozygous mutations in the inverted formin 2 (INF2) gene are related to secondary focal segmental glomerulosclerosis (FSGS), a rare secondary disease associated with rapidly progressive renal failure. Case presentation We report a patient with familial autosomal INF2 mutation...

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Bibliographic Details
Main Authors: Wenbo Zhao, Xinxin Ma, Xiaohao Zhang, Dan Luo, Jun Zhang, Ming Li, Zengchun Ye, Hui Peng
Format: Article
Language:English
Published: BMC 2021-02-01
Series:BMC Nephrology
Subjects:
INF2
Mutation analysis
End-stage renal disease
Kidney transplant
Online Access:https://doi.org/10.1186/s12882-021-02254-9

Internet

https://doi.org/10.1186/s12882-021-02254-9

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