Concepedia

Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohort

Shuzhen Sun, Linan Xu, Yunli Bi, Jing Wang, Zhiqing Zhang, Xiaoshan Tang, Qi Cao, Yi­hui Zhai, Jing Chen, Xiaoyan Fang,

European Journal of Medical Genetics · 2020 · 14 citations · 6 references

DOIFull text

Open access

Abstract

Screening for WT1 mutations should be performed in children with Wilms' tumor, proteinuria/SRNS or CKD. Early diagnosis of WT1 nephropathy through clinical and genetic findings is warranted.

References

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