An overview of the multi-pronged approach in the diagnosis of Alport syndrome for 22 children in Northeast China

BACKGROUND: Alport syndrome (AS) is a kind of progressive hereditary nephritis induced by mutations of different genes that encode collagen IV. The affected individuals usually develop hematuria during childhood, accompanying with gradual deterioration of renal functions. In this study, the multi-pr...

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Bibliographic Details
Published in:BMC Nephrol
Main Authors: Zhang, Li, Sun, Bai-chao, Zhao, Bing-gang, Ma, Qing-shan
Format: Artigo
Language:Inglês
Published: BioMed Central 2020
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC7379802/
https://ncbi.nlm.nih.gov/pubmed/32703181
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-020-01962-y
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