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

CONCLUSION: 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.
PMID: 32891756 [PubMed - as supplied by publisher]

Source: European Journal of Medical Genetics - September 2, 2020 Category: Genetics & Stem Cells Authors: Sun S, Xu L, Bi Y, Wang J, Zhang Z, Tang X, Cao Q, Zhai Y, Chen J, Fang X, Liu J, Fang Y, Xiang T, Qian Y, Wu B, Wang H, Zhou W, Shen J, Dong K, Liu X, Zheng B, Zhang A, Wang X, Wu Y, Ma D, Shen Q, Rao J, Xu H Tags: Eur J Med Genet Source Type: research